Skip to main content

Longevity of the Immune Response and Memory to Blood-Stage Malaria Infection

  • Chapter
Immunology and Immunopathogenesis of Malaria

Part of the book series: Current Topics in Microbiology and Immunology ((CT MICROBIOLOGY,volume 297))

Abstract

Immunity to malaria develops slowly with protection against the parasite lagging behind protection against disease symptoms. The data on the longevity of protective immune responses are sparse.However, studies of antibody responses associated with protection reveal that they consist of a short- and a long-lived component. Compared with the antibody levels observed in other infection and immunization systems, the levels of the short-lived antibody compartment drop below the detectable thresholdwithunusual rapidity. Theprevalenceof long-livedantibodies is comparable to that seen after bacterial and protozoan infections. There is even less available data concerning T cell longevity in malaria infection, but what there is seems to indicate that T cell memory is short in the absence of persistent antigen. In general, the degree and duration of parasite persistence represent a major factor determining how immune response longevity and protection correlate. The predilection for short-lived immune responses in malaria infection could be caused by a number of mechanisms resulting from the interplay of normal regulatory mechanisms of the immune system and immune evasion by the parasite. In conclusion, it appears that the parasite-host relationship has developed to favor some short-lived responses,which allowthe host to survivewhile allowing the parasite to persist.Anti-malarialimmune responses present a complexpicture, andmany aspects of regulationandlongevity of the response require further research.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Abdel-Latif MS, Dietz K, Issifou S, Kremsner PG, Klinkert MQ (2003) Antibodies to Plasmodium falciparum rifin proteins are associated with rapid parasite clearance and asymptomatic infections. Infect Immun 71:6229–6233

    Article  PubMed  CAS  Google Scholar 

  • Achidi EA, Perlmann H, Berzins K (1995) Asymptomatic malaria parasitaemia and seroreactivities to Plasmodium falciparum antigens in blood donors from Ibadan, south-western Nigeria. Ann Trop Med Parasitol 89:601–610

    PubMed  CAS  Google Scholar 

  • Achtman H, Khan M, MacLennan IC, Langhorne J (2003) Plasmodium chabaudi chabaudi infection in mice induces strong B cell responses and striking but temporary changes in splenic cell distribution. J Immunol 171:317–324

    PubMed  CAS  Google Scholar 

  • Ahmed R, Gray D (1996) Immunological memory and protective immunity: understanding their relation. Science 272:54–60

    PubMed  CAS  Google Scholar 

  • Akilesh S, Petkova S, Sproule TJ, Shaffer DJ, Christianson GJ, Roopenian D (2004) The MHC class I-like Fc receptor promotes humorally mediated autoimmune disease. J Clin Invest 113:1328–1333

    Article  PubMed  CAS  Google Scholar 

  • al-Yaman F, Genton B, Anders RF, Falk M, Triglia T, Lewis D, Hii J, Beck HP, Alpers MP (1994) Relationship between humoral response to Plasmodium falciparum merozoite surface antigen-2 and malaria morbidity in a highly endemic area of Papua New Guinea. Am J Trop Med Hyg 51:593–602

    Google Scholar 

  • al-Yaman F, Genton B, Kramer KJ, Taraika J, Chang SP, Hui GS, Alpers MP (1995) Acquired antibody levels to Plasmodium falciparum merozoite surface antigen 1 in residents of a highly endemic area of Papua New Guinea. Trans R Soc Trop Med Hyg 89:555–559

    Google Scholar 

  • al-Yaman F, Genton B, Reeder JC, Anders RF, Smith T, Alpers MP (1997) Reduced risk of clinical malaria in children infected with multiple clones of Plasmodium falciparum in a highly endemic area: a prospective community study. Trans R Soc Trop Med Hyg 91:602–605

    Google Scholar 

  • Anam K, Afrin F, Banerjee D, Pramanik N, Guha SK, Goswami RP, Saha SK, Ali N (1999) Differential decline in Leishmania membrane antigen-specific immunoglobulin G (IgG), IgM, IgE, and IgG subclass antibodies in Indian kala-azar patients after chemotherapy. Infect Immun 67:6663–6669

    PubMed  CAS  Google Scholar 

  • Anders RF (1986) Multiple cross-reactivities amongst antigens of Plasmodium falciparum impair the development of protective immunity against malaria. Parasite Immunol 8:529–539

    PubMed  CAS  Google Scholar 

  • Anders RF, Crewther PE, Edwards S, Margetts M, Matthew ML, Pollock B, Pye D (1998) Immunisation with recombinant AMA-1 protects mice against infection with Plasmodium chabaudi. Vaccine 16:240–247

    Article  PubMed  CAS  Google Scholar 

  • Andrade SG, Freitas LA, Peyrol S, Pimentel AR, Sadigursky M (1991) Experimental chemotherapy of Trypanosoma cruzi infection: persistence of parasite antigens and positive serology in parasitologically cured mice. Bull World Health Organ 69:191–197

    PubMed  CAS  Google Scholar 

  • Artavanis-Tsakonas K, Tongren JE, Riley EM (2003) The war between the malaria parasite and the immune system: immunity, immunoregulation and immunopathology. Clin Exp Immunol 133:145–152

    Article  PubMed  CAS  Google Scholar 

  • Asahi T, Ueda K, Hidaka Y, Miyazaki C, Tanaka Y, Nishima S (1997) Twenty-three-year follow-up study of rubella antibodies after immunization in a closed population, and serological response to revaccination. Vaccine 15:1791–1795

    Article  PubMed  CAS  Google Scholar 

  • Astagneau P, Chougnet C, Lepers JP, Danielle M, Andriamangatiana-Rason MD, Deloron P (1994) Antibodies to the 4-mer repeat of the ring-infected erythrocyte surface antigen (Pf155/RESA) protect against Plasmodium falciparum malaria. Int J Epidemiol 23:169–175

    PubMed  CAS  Google Scholar 

  • Baird JK (1998) Age-dependent characteristics of protection v. susceptibility to Plasmodium falciparum. Ann Trop Med Parasitol 92:367–390

    Article  PubMed  CAS  Google Scholar 

  • Baird JK, Purnomo, Basri H, Bangs MJ, Andersen EM, Jones TR, Masbar S, Harjosuwarno S, Subianto B, Arbani PR (1993) Age-specific prevalence of Plasmodium falciparum among six populations with limited histories of exposure to endemic malaria. Am J Trop Med Hyg 49:707–719.

    PubMed  CAS  Google Scholar 

  • Barnwell JW, Howard RJ, Miller LH(1982) Altered expression of Plasmodium knowlesi variant antigen on the erythrocyte membrane in splenectomized rhesus monkeys. J Immunol 128:224–226

    PubMed  CAS  Google Scholar 

  • Baruch DI, Ma XC, Pasloske B, Howard RJ, Miller LH (1999) CD36 peptides that block cytoadherence define the CD36 binding region for Plasmodium falciparum-infected erythrocytes. Blood 94:2121–2127

    PubMed  CAS  Google Scholar 

  • Baruch DI, Pasloske BL, Singh HB, Bi X, Ma XC, Feldman M, Taraschi TF, Howard RJ (1995) Cloning the P. falciparum gene encoding PfEMP1, a malarial variant antigen and adherence receptor on the surface of parasitized human erythrocytes. Cell 82:77–87

    Article  PubMed  CAS  Google Scholar 

  • Bernasconi NL, Traggiai E, Lanzavecchia A (2002) Maintenance of serological memory by polyclonal activation of human memory B cells. Science 298:2199–2202

    Article  PubMed  CAS  Google Scholar 

  • Berzins K, Perlmann H, Wahlin B, Ekre HP, Hogh B, Petersen E, Wellde B, Schoenbechler M, Williams J, Chulay J, al. e (1991) Passive immunization of Aotus monkeys with human antibodies to the Plasmodium falciparum antigen Pf155/RESA. Infect Immun 59: 1500–1506

    PubMed  CAS  Google Scholar 

  • Bilsborough J, Carlisle M, Good MF (1993) Identification of Caucasian CD4 T cell epitopes on the circumsporozoite protein of Plasmodium vivax. T cell memory. J Immunol 151:890–899

    CAS  Google Scholar 

  • Borrow R, Goldblatt D, Andrews N, Richmond P, Southern J, Miller E (2001) Influence of prior meningococcal C polysaccharide vaccination on the response and generation of memory after meningococcal C conjugate vaccination in young children. J Infect Dis 184:377–380

    PubMed  CAS  Google Scholar 

  • Borrow R, Goldblatt D, Andrews N, Southern J, Ashton L, Deane S, Morris R, Cartwright K, Miller E (2002) Antibody persistence and immunological memory at age 4 years after meningococcal group C conjugate vaccination in children in the United kingdom. J Infect Dis 186:1353–1357

    Article  PubMed  Google Scholar 

  • Boutlis CS, Gowda DC, Naik RS, Maguire GP, Mgone CS, Bockarie MJ, Lagog M, Ibam E, Lorry K, Anstey NM (2002) Antibodies to Plasmodium falciparum glycosylphosphatidylinositols: inverse association with tolerance of parasitemia in Papua New Guinean children and adults. Infect Immun 70:5052–5057

    Article  PubMed  CAS  Google Scholar 

  • Braga EM, Barros RM, Reis TA, Fontes CJ, Morais CG, Martins MS, Krettli AU (2002) Association of the IgG response to Plasmodium falciparum merozoite protein (C-terminal 19 kD) with clinical immunity to malaria in the Brazilian Amazon region. Am J Trop Med Hyg 66:461–466

    PubMed  CAS  Google Scholar 

  • Braga EM, Fontes CJF, Krettli AU (1998) Persistence of humoral response against sporozoite and blood-stage malaria antigens 7 years after a brief exposure to Plasmodium vivax. J Infect Dis 177:1132–1135

    PubMed  CAS  Google Scholar 

  • Branch OH, Udhayakumar V, Hightower AW, Oloo AJ, Hawley WA, Nahlen BL, Bloland PB, Kaslow DC, Lal AA (1998) A longitudinal investigation of IgG and IgM antibody responses to the merozoite surface protein-1 19-kilodalton domain of Plasmodium falciparum in pregnant women and infants: associations with febrile illness, parasitemia, and anemia. Am J Trop Med Hyg 58:211–219

    PubMed  CAS  Google Scholar 

  • Brink R, Goodnow CC, Crosbie J, Adams E, Eris J, Mason DY, Hartley SB, Basten A (1992) Immunoglobulin M and D antigen receptors are both capable of mediating B lymphocyte activation, deletion, or anergy after interaction with specific antigen. J Exp Med 176:991–1005

    Article  PubMed  CAS  Google Scholar 

  • Brögger LC, Mathews HM, Storey J, Ashkar TS, Molineaux L (1978) Changing patterns in the humoral immune response to malaria before, during, and after the application of control measures: a longitudinal study in the West African savanna. Bull World Health Organ 56:579–600

    PubMed  Google Scholar 

  • Brown AE, Webster HK, Krinchai K, Gordon DM, Wirtz RA, Permpanich B (1991) Characteristics of natural antibody responses to the circumsporozoite protein of Plasmodium vivax. Am J Trop Med Hyg 44:21–27

    PubMed  CAS  Google Scholar 

  • Brown KN, Brown IN (1965) Immunity to malaria: antigenic variation in chronic infections of Plasmodium knowlesi. Nature 208:1286–1288

    PubMed  CAS  Google Scholar 

  • Bull PC, Lowe BS, Kaleli N, Njuga F, Kortok M, Ross A, Ndungu F, Snow RW, Marsh K (2002) Plasmodium falciparum infections are associated with agglutinating antibodies to parasite-infected erythrocyte surface antigens among healthy Kenyan children. J Infect Dis 185:1688–1691

    Article  PubMed  Google Scholar 

  • Bull PC, Lowe BS, Kortok M, Molyneux CS, Newbold CI, Marsh K (1998) Parasite antigens on the infected red cell surface are targets for naturally acquired immunity to malaria. Nat Med 4:358–360

    Article  PubMed  CAS  Google Scholar 

  • Calvo PA, Daly TM, Long CA (1996) Both epidermal growth factor-like domains of the merozoite surface protein-1 from Plasmodium yoelii are required for protection from malaria. Ann N Y Acad Sci 797:260–262

    PubMed  CAS  Google Scholar 

  • Carlson J, Helmby H, Hill AV, Brewster D, Greenwood BM, Wahlgren M (1990) Human cerebral malaria: association with erythrocyte rosetting and lack of anti-rosetting antibodies. Lancet 336:1457–1460

    Article  PubMed  CAS  Google Scholar 

  • Carlton JM, Angiuoli SV, Suh BB, Kooij TW, Pertea M, Silva JC, Ermolaeva MD, Allen JE, Selengut JD, Koo HL, Peterson JD, Pop M, Kosack DS, Shumway MF, Bidwell SL, Shallom SJ, van Aken SE, Riedmuller SB, Feldblyum TV, Cho JK, Quackenbush J, Sedegah M, Shoaibi A, Cummings LM, Florens L, Yates JR, Raine JD, Sinden RE, Harris MA, Cunningham DA, Preiser PR, Bergman LW, Vaidya AB, van Lin LH, Janse CJ, Waters AP, Smith HO, White OR, Salzberg SL, Venter JC, Fraser CM, Hoffman SL, Gardner MJ, Carucci DJ (2002) Genome sequence and comparative analysis of the model rodent malaria parasite Plasmodium yoelii yoelii. Nature 419:512–519

    Article  PubMed  CAS  Google Scholar 

  • Cavanagh DR, Elhassan IM, Roper C, Robinson VJ, Giha H, Holder AA, Hviid L, Theander TG, Arnot DE, McBride JS (1998) A longitudinal study of type-specific antibody responses to Plasmodium falciparum merozoite surface protein-1 in an area of unstable malaria in Sudan. J Immunol 161:347–359

    PubMed  CAS  Google Scholar 

  • Cawthraw SA, Feldman RA, Sayers AR, Newell DG (2002) Long-term antibody responses following human infection with Campylobacter jejuni.Clin Exp Immunol 130:101–106

    Article  PubMed  CAS  Google Scholar 

  • Chang SP, Case SE, Gosnell WL, Hashimoto A, Kramer KJ, Tam LQ, Hashiro CQ, Nikaido CM, Gibson HL, Lee-Ng CT, Barr PJ, Yokota BT, Hut GS (1996) A recombinant baculovirus 42-kilodalton C-terminal fragment of Plasmodium falciparum merozoite surface protein 1 protects Aotus monkeys against malaria. Infect Immun 64:253–261

    PubMed  CAS  Google Scholar 

  • Chizzolini C, Dupont A, Akue JP, Kaufmann MH, Verdini AS, Pessi A, Del Giudice G (1988) Natural antibodies against three distinct and defined antigens of Plasmodium falciparum in residents of a mesoendemic area in Gabon. Am J Trop Med Hyg 39:150–156

    PubMed  CAS  Google Scholar 

  • Ciofu O, Petersen TD, Jensen P, Hoiby N (1999) Avidity of anti-P. aeruginosa antibodies during chronic infection in patients with cystic fibrosis. Thorax 54:141–144

    Article  PubMed  CAS  Google Scholar 

  • Ciuca M, Ballif L, Chelarescu-Vieru M (1934) Immunity in malaria. Trans R Soc Trop Med Hyg 27:619–622

    Article  Google Scholar 

  • Cohen S, McGregor IA, Carrington S (1961) Gamma-globulin and acquired immunity to human malaria. Nature 192:733–737

    PubMed  CAS  Google Scholar 

  • Collins WE, Jeffery GM (1999) A retrospective examination of secondary sporozoiteand trophozoite-induced infections with Plasmodium falciparum: development of parasitologic and clinical immunity following secondary infection. Am J Trop Med Hyg 61:20–35

    PubMed  CAS  Google Scholar 

  • Contamin H, Fandeur T, Rogier C, Bonnefoy S, Konate L, Trape JF, Mercereau-Puijalon O (1996) Different genetic characteristics of Plasmodium falciparum isolates collected during successive clinical malaria episodes in Senegalese children. Am J Trop Med Hyg 54:632–643

    PubMed  CAS  Google Scholar 

  • Conway DJ (1997) Natural selection on polymorphic malaria antigens and the search for a vaccine. Parasitol Today 13:26–29

    Article  PubMed  CAS  Google Scholar 

  • Crotty S, Felgner P, Davies H, Glidewell J, Villarreal L, Ahmed R (2003) Cutting edge: long-term B cell memory in humans after smallpox vaccination. J Immunol 171:4969–4973

    PubMed  CAS  Google Scholar 

  • Daly TM, Long CA (1995) Humoral response to a carboxyl-terminal region of the merozoite surface protein-1 plays a predominant role in controlling blood-stage infection in rodent malaria. J Immunol 155:236–243

    PubMed  CAS  Google Scholar 

  • Daubersies P, Sallenave-Sales S, Magne S, Trape JF, Contamin H, Fandeur T, Rogier C, Mercereau-Puijalon O, Druilhe P (1996) Rapid turnover of Plasmodium falciparum populations in asymptomatic individuals living in a high transmission area. Am J Trop Med Hyg 54:18–26

    PubMed  CAS  Google Scholar 

  • Davidkin I, Valle M, Julkunen I (1995) Persistence of anti-mumps virus antibodies after a two-dose MMR vaccination. A nine-year follow-up. Vaccine 13:1617–1622

    Article  PubMed  CAS  Google Scholar 

  • del Portillo HA, Fernandez-Becerra C, Bowman S, Oliver K, Preuss M, Sanchez CP, Schneider NK, Villalobos JM, Rajandream MA, Harris D, Pereira da Silva LH, Barrell B, Lanzer M (2001) A superfamily of variant genes encoded in the subtelomeric region of Plasmodium vivax. Nature 410:839–842

    PubMed  Google Scholar 

  • Deloron P, Chougnet C (1992) Is immunity to malaria really short-lived? Parasitol Today 8:375–378

    Article  PubMed  CAS  Google Scholar 

  • Di Perri G, Bonora S, Vento S, Concia E (1995) Naturally acquired immunity to Plasmodium falciparum. Parasitol Today 11:346–347

    PubMed  Google Scholar 

  • Diggs CL, Hines F, Wellde BT (1995) Plasmodium falciparum: passive immunization of Aotus lemurinus griseimembra with immune serum. Exp Parasitol 80:291–296

    Article  PubMed  CAS  Google Scholar 

  • Dodoo D, Staalsoe T, Giha H, Kurtzhals JA, Akanmori BD, Koram K, Dunyo S, Nkrumah FK, Hviid L, Theander TG (2001) Antibodies to variant antigens on the surfaces of infected erythrocytes are associated with protection from malaria in Ghanaian children. Infect Immun 69:3713–3718

    Article  PubMed  CAS  Google Scholar 

  • Dodoo D, Theander TG, Kurtzhals JA, Koram K, Riley E, Akanmori BD, Nkrumah FK, Hviid L (1999) Levels of antibody to conserved parts of Plasmodium falciparum merozoite surface protein 1 in Ghanaian children are not associated with protection from clinical malaria. Infect Immun 67:2131–2137

    PubMed  CAS  Google Scholar 

  • Donati D, Zhang LP, Chen Q, Chene A, Flick K, Nystrom M, Wahlgren M, Bejarano MT (2004) Identification of a polyclonal B-cell activator in Plasmodium falciparum. Infect Immun 72:5412–5418

    Article  PubMed  CAS  Google Scholar 

  • Druilhe P, Pérignon JL (1994) Immune mechanisms underlying the premunition against Plasmodium falciparum malaria. Mem Inst Oswaldo Cruz 89:51–53

    PubMed  Google Scholar 

  • Druilhe P, Pradier O, Marc JP, Miltgen F, Mazier D, Parent G (1986) Levels of antibodies to Plasmodium falciparum sporozoite surface antigens reflect malaria transmission rates and are persistent in the absence of reinfection. Infect Immun 53: 393–397.

    PubMed  CAS  Google Scholar 

  • Egan AF, Morris J, Barnish G, Allen S, Greenwood BM, Kaslow DC, Holder AA, Riley EM (1996) Clinical immunity to Plasmodium falciparum malaria is associated with serum antibodies to the 19-kDa C-terminal fragment of the merozoite surface antigen, PfMSP-1 J Infect Dis 173:765–769.

    PubMed  CAS  Google Scholar 

  • Eling WMC (1980) Plasmodium berghei: premunition, sterile immunity, and loss of immunity in mice. Exp Parasitol 49:89–96

    Article  PubMed  CAS  Google Scholar 

  • Ericsson M, Sandstrom G, Sjostedt A, Tarnvik A (1994) Persistence of cell-mediated immunity and decline of humoral immunity to the intracellular bacterium Francisella tularensis 25 years after natural infection. J Infect Dis 170:110–114

    PubMed  CAS  Google Scholar 

  • Farnert A, Snounou G, Rooth I, Bjorkman A (1997) Daily dynamics of Plasmodium falciparum subpopulations in asymptomatic children in a holoendemic area. Am J Trop Med Hyg 56:538–547

    PubMed  CAS  Google Scholar 

  • Ferreira MU, Katzin AM (1995) The assessment of antibody affinity distribution by thiocyanate elution: a simple dose-response approach. J Immunol Methods 187:297–305

    Article  PubMed  CAS  Google Scholar 

  • Ferreira MU, Kimura EA, De Souza JM, Katzin AM (1996) The isotype composition and avidity of naturally acquired anti-Plasmodium falciparum antibodies: differential patterns in clinically immune Africans and Amazonian patients. Am J Trop Med Hyg 55:315–323

    PubMed  CAS  Google Scholar 

  • Flanagan KL, Mwangi T, Plebanski M, Odhiambo K, Ross A, Sheu E, Kortok M, Lowe B, Marsh K, Hill AV (2003) Ex vivo interferon-gamma immune response to thrombospondin-related adhesive protein in coastal Kenyans: longevity and risk of Plasmodium falciparum infection. Am J Trop Med Hyg 68:421–430

    PubMed  CAS  Google Scholar 

  • Fonjungo PN, Elhassan IM, Cavanagh DR, Theander TG, Hviid L, Roper C, Arnot DE, McBride JS (1999) A longitudinal study of human antibody responses to Plasmodium falciparum rhoptry-associated protein 1 in a region of seasonal and unstable malaria transmission. Infect Immun 67:2975–2985

    PubMed  CAS  Google Scholar 

  • Früh K, Doumbo O, Muller HM, Koita O, McBride J, Crisanti A, Toure Y, Bujard H (1991) Human antibody response to the major merozoite surface antigen of Plasmodium falciparum is strain specific and short-lived. Infect Immun 59:1319–1324

    PubMed  Google Scholar 

  • Galinski MR, Corredor V (2004) Variant antigen expression in malaria infections: posttranscriptional gene silencing, virulence and severe pathology. Mol Biochem Parasitol 134:17–25

    Article  PubMed  CAS  Google Scholar 

  • Garcia S, DiSanto J, Stockinger B (1999) Following the development of a CD4 T cell response in vivo: from activation to memory formation. Immunity 11:163–171

    Article  PubMed  CAS  Google Scholar 

  • Garraud O, Perraut R, Diouf A, Nambei WS, Tall A, Spiegel A, Longacre S, Kaslow DC, Jouin H, Mattei D, Engler GM, Nutman TB, Riley EM, Mercereau-Puijalon O (2002) Regulation of antigen-specific immunoglobulin G subclasses in response to conserved and polymorphic Plasmodium falciparum antigens in an in vitro model. Infect Immun 70:2820–2827

    Article  PubMed  CAS  Google Scholar 

  • Giha HA, Staalsoe T, Dodoo D, Elhassan IM, Roper C, Satti GM, Arnot DE, Theander TG, Hviid L (1999) Nine-year longitudinal study of antibodies to variant antigens on the surface of Plasmodium falciparum-infected erythrocytes. Infect Immun 67:4092–4098

    PubMed  CAS  Google Scholar 

  • Giha HA, Theander TG, Staalso T, Roper C, Elhassan IM, Babiker H, Satti GM, Arnot DE, Hviid L (1998) Seasonal variation in agglutination of Plasmodium falciparum-infected erythrocytes. Am J Trop Med Hyg 58:399–405

    PubMed  CAS  Google Scholar 

  • Goldblatt D, Borrow R, Miller E (2002) Natural and vaccine-induced immunity and immunologic memory to Neisseria meningitidis serogroup C in young adults. J Infect Dis 185:397–400

    Article  PubMed  Google Scholar 

  • Gozalo A, Lucas C, Cachay M, Wellde BT, Hall T, Bell B, Wood J, Watts D, Wooster M, Lyon JA, Moch JK, Haynes JD, Williams JS, Holland C, Watson E, Kester KE, Kaslow DC, Ballou WR (1998) Passive transfer of growth-inhibitory antibodies raised against yeast-expressed recombinant Plasmodium falciparum merozoite surface protein-1(19). Am J Trop Med Hyg 59:991–997

    PubMed  CAS  Google Scholar 

  • Gray D, Skarvall H (1988) B-cell memory is short-lived in the absence of antigen. Nature 336:70–73

    Article  PubMed  CAS  Google Scholar 

  • Greenwood BM (1974) Possible role of a B-cell mitogen in hypergammaglobulinaemia in malaria and trypanosomiasis. Lancet 1:435–436

    PubMed  CAS  Google Scholar 

  • Greenwood BM, David PH, Otoo-Forbes LN, Allen SJ, Alonso PL, Armstrong Schellenberg JR, Byass P, Hurwitz M, Menon A, Snow RW (1995) Mortality and morbidity from malaria after stopping malaria chemoprophylaxis. Trans R Soc Trop Med Hyg 89:629–633

    Article  PubMed  CAS  Google Scholar 

  • Grun JL, Weidanz WP (1983) Antibody-independent immunity to reinfection malaria in B-cell-deficient mice. Infect Immun 41:1197–1204

    PubMed  CAS  Google Scholar 

  • Gupta S, Snow RW, Donnelly CA, Marsh K, Newbold C (1999) Immunity to non-cerebral severe malaria is acquired after one or two infections. Nat Med 5:340–343

    PubMed  CAS  Google Scholar 

  • Gysin J, Moisson P, Pereira da Silva L, Druilhe P (1996) Antibodies from immune African donors with a protective effect in Plasmodium falciparum human infection are also able to control asexual blood forms of the parasite in Saimiri monkeys. Res Immunol 147:397–401

    PubMed  CAS  Google Scholar 

  • Hammarlund E, Lewis MW, Hansen SG, Strelow LI, Nelson JA, Sexton GJ, Hanifin JM, Slifka MK (2003) Duration of antiviral immunity after smallpox vaccination. Nat Med 9:1131–1137

    Article  PubMed  CAS  Google Scholar 

  • Hirunpetcharat C, Tian JH, Kaslow DC, van Rooijen N, Kumar S, Berzofsky JA, Miller LH, Good MF (1997) Complete protective immunity induced in mice by immunization with the 19-kilodalton carboxyl-terminal fragment of the merozoite surface protein-1 (MSP1[19]) of Plasmodium yoelii expressed in Saccharomyces cerevisiae: correlation of protection with antigen-specific antibody titer, but not with effector CD4+ T cells. J Immunol 159:3400–3411

    PubMed  CAS  Google Scholar 

  • Hogh B, Petersen E, Dziegiel M, David K, Hanson A, Borre M, Holm A, Vuust J, Jepsen S (1992) Antibodies to a recombinant glutamate-rich Plasmodium falciparum protein: evidence for protection of individuals living in a holoendemic area of Liberia. Am J Trop Med Hyg 46:307–313

    PubMed  CAS  Google Scholar 

  • Hughes MK, Hughes AL (1995) Natural selection on Plasmodium surface proteins. Mol Biochem Parasitol 71:99–113

    Article  PubMed  CAS  Google Scholar 

  • Hviid L, Kurtzhals JA, Goka BQ, Oliver-Commey JO, Nkrumah FK, Theander TG (1997) Rapid reemergence of T cells into peripheral circulation following treatment of severe and uncomplicated Plasmodium falciparum malaria. Infect Immun 65:4090–4093

    PubMed  CAS  Google Scholar 

  • Hviid L, Staalsoe T (2004) Malaria immunity in infants: a special case of a general phenomenon? Trends Parasitol 20:66–72

    Article  PubMed  CAS  Google Scholar 

  • Jacob J, Kassir R, Kelsoe G (1991) In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. I. The architecture and dynamics of responding cell populations. J Exp Med 173:1165–1175

    Article  PubMed  CAS  Google Scholar 

  • Jakobsen PH, Kurtzhals JA, Riley EM, Hviid L, Theander TG, Morris-Jones S, Jensen JB, Bayoumi RA, Ridley RG, Greenwood BM (1997) Antibody responses to Rhoptry-Associated Protein-1 (RAP-1) of Plasmodium falciparum parasites in humans from areas of different malaria endemicity. Parasite Immunol 19:387–393

    Article  PubMed  CAS  Google Scholar 

  • Janssen CS, Barrett MP, Turner CM, Phillips RS (2002) A large gene family for putative variant antigens shared by human and rodent malaria parasites. Proc R Soc Lond B Biol Sci 269:431–436

    Article  CAS  Google Scholar 

  • Jarra W, Hills LA, March JC, Brown KN (1986) Protective immunity to malaria. Studies with cloned lines of Plasmodium chabaudi chabaudi and P. berghei in CBA/Ca mice. II. The effectiveness and inter-or intra-species specificity of the passive transfer of immunity with serum. Parasite Immunol 8:239–254

    PubMed  CAS  Google Scholar 

  • John CC, Ouma JH, Sumba PO, Hollingdale MR, Kazura JW, King CL (2002) Lymphocyte proliferation and antibody responses to Plasmodium falciparum liver-stage antigen-1 in a highland area of Kenya with seasonal variation in malaria transmission. Am J Trop Med Hyg 66:372–378

    PubMed  Google Scholar 

  • Kaneko A (1999).Malaria on islands: human and parasite diversities and implications for malaria control in Vanuatu. In “Department of Medicine, Unit of Infectious Diseases”. Karolinska Institutet, Karolinska Hospital, Stockholm.

    Google Scholar 

  • Kaneko A, Taleo G, Kalkoa M, Yamar S, Kobayakawa T, Björkman A (2000) Malaria eradication on islands. Lancet 356:1560–1564

    Article  PubMed  CAS  Google Scholar 

  • Karrer U, Lopez-Macias C, Oxenius A, Odermatt B, Bachmann MF, Kalinke U, Bluethmann H, Hengartner H, Zinkernagel RM (2000) Antiviral B cell memory in the absence of mature follicular dendritic cell networks and classical germinal centers in TNFR1-/- mice. J Immunol 164:768–778

    PubMed  CAS  Google Scholar 

  • Kassiotis G, Garcia S, Simpson E, Stockinger B (2002) Impairment of immunological memory in the absence of MHC despite survival of memory T cells. Nat Immunol 3:244–250

    Article  PubMed  CAS  Google Scholar 

  • Kinyanjui SM, Mwangi, T, Bull PC, Newbold CI, Marsh K (2004) Protection against clinical malaria by heterologous immunoglobulin G antibodies against malaria-infected erythrocyte variant surface antigens requires interaction with asymptomatic infections. J Infect Dis 190:1527–1533

    Article  PubMed  Google Scholar 

  • Kinyanjui SM, Bull P, Newbold CI, Marsh K (2003) Kinetics of antibody responses to Plasmodium falciparum-infected erythrocyte variant surface antigens. J Infect Dis 187:667–674

    Article  PubMed  CAS  Google Scholar 

  • Kundig TM, Bachmann MF, Oehen S, Hoffmann UW, Simard JJ, Kalberer CP, Pircher H, Ohashi PS, Hengartner H, Zinkernagel RM (1996) On the role of antigen in maintaining cytotoxic T-cell memory. Proc Natl Acad Sci U S A 93:9716–9723

    Article  PubMed  CAS  Google Scholar 

  • Langhorne J, Cross C, Seixas E, Li C, von der Weid T (1998) A role for B cells in the development of T cell helper function in a malaria infection in mice. Proc Natl Acad Sci USA 95:1730–1734

    Article  PubMed  CAS  Google Scholar 

  • Langhorne J, Kim KJ, Asofsky R (1985) Distribution of immunoglobulin isotypes in the nonspecific B-cell response induced by infection with Plasmodium chabaudi adami and Plasmodium yoelii. Cell Immunol 90:251–257

    Article  PubMed  CAS  Google Scholar 

  • Langhorne J, Simon-Haarhaus B (1991) Differential T cell responses to Plasmodium chabaudi chabaudi in peripheral blood and spleens of C57BL/6 mice during infection. J Immunol 146:2771–2775

    PubMed  CAS  Google Scholar 

  • LaRussa PS, Gershon AA, Steinberg SP, Chartrand SA (1990) Antibodies to varicella-zoster virus glycoproteins I, II, and III in leukemic and healthy children. J Infect Dis 162: 627–633

    PubMed  CAS  Google Scholar 

  • Ling IT, Ogun SA, Holder AA (1995) The combined epidermal growth factor-like modules of Plasmodium yoelii Merozoite Surface Protein-1 are required for a protective immune response to the parasite. Parasite Immunol 17:425–433

    PubMed  CAS  Google Scholar 

  • Luty AJ, Ulbert S, Lell B, Lehman L, Schmidt-Ott R, Luckner D, Greve B, Matousek P, Schmid D, Herbich K, Dubois B, Deloron P, Kremsner PG (2000) Antibody responses to Plasmodium falciparum: evolution according to the severity of a prior clinical episode and association with subsequent reinfection. Am J Trop Med Hyg 62:566–572

    PubMed  CAS  Google Scholar 

  • MacLennan IC, Garcia de Vinuesa C, Casamayor-Palleja M (2000) B-cell memory and the persistence of antibody responses. Philos Trans R Soc Lond B Biol Sci 355:345–350

    PubMed  CAS  Google Scholar 

  • MacLennan ICM (1995) B cells. Avoiding autoreactivity. Nature 375:281

    Article  PubMed  CAS  Google Scholar 

  • Magesa SM, Mdira KY, Babiker HA, Alifrangis M, Farnert A, Simonsen PE, Bygbjerg IC, Walliker D, Jakobsen PH (2002) Diversity of Plasmodium falciparum clones infecting children living in a holoendemic area in north-eastern Tanzania. Acta Trop 84:83–92

    PubMed  CAS  Google Scholar 

  • Maley SW, Buxton D, Thomson KM, Schriefer CE, Innes EA (2001) Serological analysis of calves experimentally infected with Neospora caninum: a 1-year study. Vet Parasitol 96:1–9

    PubMed  CAS  Google Scholar 

  • Mallet E, Fabre P, Pines E, Salomon H, Staub T, Schodel F, Mendelman P, Hessel L, Chryssomalis G, Vidor E, Hoffenbach A (2000) Immunogenicity and safety of a new liquid hexavalent combined vaccine compared with separate administration of reference licensed vaccines in infants. Pediatr Infect Dis J 19: 1119–1127

    PubMed  CAS  Google Scholar 

  • Manz RA, Radbruch A (2002) Plasma cells for a lifetime? Eur J Immunol 32:923–927

    Article  PubMed  CAS  Google Scholar 

  • Manz RA, Thiel A, Radbruch A (1997) Lifetime of plasma cells in the bone marrow. Nature 388:133–134

    Article  PubMed  CAS  Google Scholar 

  • Maple PA, Jones CS, Wall EC, Vyseb A, Edmunds WJ, Andrews NJ, Miller E (2000) Immunity to diphtheria and tetanus in England and Wales. Vaccine 19:167–173

    PubMed  CAS  Google Scholar 

  • Marsh K (1992) Malaria-a neglected disease? Parasitology 104: S53–S69

    Article  PubMed  Google Scholar 

  • Marsh K, Otoo L, Hayes RJ, Carson DC, Greenwood BM (1989) Antibodies to blood stage antigens of Plasmodium falciparum in rural Gambians and their relation to protection against infection. Trans R Soc Trop Med Hyg 83:293–303

    Article  PubMed  CAS  Google Scholar 

  • Martin SW, Goodnow CC (2002) Burst-enhancing role of the IgG membrane tail as a molecular determinant of memory. Nat Immunol 3:182–188

    Article  PubMed  CAS  Google Scholar 

  • Maruyama M, Lam KP, Rajewsky K (2000) Memory B-cell persistence is independent of persisting immunizing antigen. Nature 407:636–642

    PubMed  CAS  Google Scholar 

  • McLean SA, Pearson CD, Phillips RS (1982) Plasmodium chabaudi: antigenic variation during recrudescent parasitaemias in mice. Exp Parasitol 54:296–302

    PubMed  CAS  Google Scholar 

  • Metzger WG, Okenu DM, Cavanagh DR, Robinson JV, Bojang KA, Weiss HA, McBride JS, Greenwood BM, Conway DJ (2003) Serum IgG3 to the Plasmodium falciparum merozoite surface protein 2 is strongly associated with a reduced prospective risk of malaria. Parasite Immunol 25:307–312

    Article  PubMed  CAS  Google Scholar 

  • Migot F, Chougnet C, Henzel D, Dubois B, Jambou R, Fievet N, Deloron P (1995) Anti-malaria antibody-producing B cell frequencies in adults after a Plasmodium falciparum outbreak in Madagascar. Clin Exp Immunol 102:529–534

    PubMed  CAS  Google Scholar 

  • Newbold C, Warn P, Black G, Berendt A, Craig A, Snow B, Msobo M, Peshu N, Marsh K (1997) Receptor-specific adhesion and clinical disease in Plasmodium falciparum. Am J Trop Med Hyg 57:389–398

    PubMed  CAS  Google Scholar 

  • O’Connor BP, Gleeson MW, Noelle RJ, Erickson LD (2003) The rise and fall of long-lived humoral immunity: terminal differentiation of plasma cells in health and disease. Immunol Rev 194:61–76

    PubMed  CAS  Google Scholar 

  • Ober RJ, Martinez C, Vaccaro C, Zhou J, Ward ES (2004) Visualizing the site and dynamics of IgG salvage by the MHC class I-related receptor, FcRn. J Immunol 172:2021–2029

    PubMed  CAS  Google Scholar 

  • Ochsenbein AF, Pinschewer DD, Sierro S, Horvath E, Hengartner H, Zinkernagel RM (2000) Protective long-term antibody memory by antigen-driven and T help-dependent differentiation of long-lived memory B cells to short-lived plasma cells independent of secondary lymphoid organs. Proc Natl Acad Sci U S A 97:13263–13268

    Article  PubMed  CAS  Google Scholar 

  • Owusu-Agyei S, Binka F, Koram K, Anto F, Adjuik M, Nkrumah F, Smith T (2002) Does radical cure of asymptomatic Plasmodium falciparum place adults in endemic areas at increased risk of recurrent symptomatic malaria? Trop Med Int Health 7:599–603

    PubMed  Google Scholar 

  • Park CG, Chwae YJ, Kim JI, Lee JH, Hur GM, Jeon BH, Koh JS, Han JH, Lee SJ, Park JW, Kaslow DC, Strickman D, Roh CS (2000) Serologic responses of Korean soldiers serving in malaria-endemic areas during a recent outbreak of Plasmodium vivax. Am J Trop Med Hyg 62:720–725

    PubMed  CAS  Google Scholar 

  • Petersen E, Hogh B, Perlmann H, Kabilan L, Troye-Blomberg M, Marbiah NT, Hanson AP, Bjorkman A, Perlmann P(1989)An epidemiological study of humoral and cell-mediated immune response to the Plasmodium falciparum antigen PF155/RESA in adult Liberians. Am J Trop Med Hyg 41:386–394

    PubMed  CAS  Google Scholar 

  • Plotkin JB, Dushoff J, Fraser HB (2004) Detecting selection using a single genome sequence of M. tuberculosis and P. falciparum. Nature 428:942–945

    Article  PubMed  CAS  Google Scholar 

  • Polley SD, Conway DJ (2001) Strong diversifying selection on domains of the Plasmodium falciparum apical membrane antigen 1 gene. Genetics 158:1505–1512

    PubMed  CAS  Google Scholar 

  • Polley SD, Mwangi T, Kocken CHM, Thomas AW, Dutta S, Lanar DE, Remarque E, Ross A, Williams T, Mwambingu G, Lowe B, Conway DJ, Marsh K (2004) Human antibodies to recombinant protein constructs of Plasmodium falciparum Apical Membrane Antigen (AMA1) and their associations with protection from malaria. Vaccine 23:718–728

    Article  PubMed  CAS  Google Scholar 

  • Pulendran B, Kannourakis G, Nouri S, Smith KG, Nossal GJ (1995) Soluble antigen can cause enhanced apoptosis of germinal-centre B cells. Nature 375:331–334.

    Article  PubMed  CAS  Google Scholar 

  • Quin SJ, Langhorne J (2001) Different regions of the malaria merozoite surface protein 1 of Plasmodium chabaudi elicit distinct T-cell and antibody isotype responses. Infect Immun 69:2245–2251.

    Article  PubMed  CAS  Google Scholar 

  • Ramasamy R, Nagendran K, Ramasamy MS (1994)Antibodies to epitopes on merozoite and sporozoite surface antigens as serologic markers of malaria transmission: studies at a site in the dry zone of Sri Lanka. Am J Trop Med Hyg 50:537–547

    PubMed  CAS  Google Scholar 

  • Recker M, Nee S, Bull PC, Kinyanjui S, Marsh K, Newbold C, Gupta S (2004) Transient cross-reactive immune responses can orchestrate antigenic variation in malaria. Nature 429:555–558

    Article  PubMed  CAS  Google Scholar 

  • Richmond P, Borrow R, Goldblatt D, Findlow J, Martin S, Morris R, Cartwright K, Miller E (2001) Ability of 3 different meningococcal C conjugate vaccines to induce immunologic memory after a single dose in UK toddlers. J Infect Dis 183: 160–163

    Article  PubMed  CAS  Google Scholar 

  • Riley EM, Allen SJ, Wheeler JG, Blackman MJ, Bennett S, Takacs B, Schonfeld HJ, Holder AA, Greenwood BM (1992) Naturally acquired cellular and humoral immune responses to the major merozoite surface antigen (PfMSP1) of Plasmodium falciparum are associated with reduced malaria morbidity. Parasite Immunol 14:321–337

    PubMed  CAS  Google Scholar 

  • Riley EM, Morris-Jones S, Blackman MJ, Greenwood BM, Holder AA (1993) A longitudinal study of naturally acquired cellular and humoral immune responses to a merozoite surface protein (MSP1) of Plasmodium falciparum in an area of seasonal malaria transmission. Parasite Immunol 15:513–524

    PubMed  CAS  Google Scholar 

  • Roberts DJ, Craig AG, Berendt AR, Pinches R, Nash G, Marsh K, Newbold CI (1992) Rapid switching to multiple antigenic and adhesive phenotypes in malaria.Nature 357:689–692

    Article  PubMed  CAS  Google Scholar 

  • Rosenberg YJ (1978) Autoimmune and polyclonal B cell responses during murine malaria. Nature 274:170–172

    Article  PubMed  CAS  Google Scholar 

  • Rotman HL, Daly TM, Long CA (1999) Plasmodium: immunization with carboxyl-terminal regions of MSP-1 protects against homologous but not heterologous blood-stage parasite challenge. Exp Parasitol 91:78–85

    Article  PubMed  CAS  Google Scholar 

  • Sabchareon A, Burnouf T, Ouattara D, Attanath P, Bouharoun-Tayoun H, Chantavanich P, Foucault C, Chongsuphajaisiddhi T, Druilhe P (1991) Parasitologic and clinical human response to immunoglobulin administration in falciparum malaria. Am J Trop Med Hyg 45:297–308

    PubMed  CAS  Google Scholar 

  • Sangster MY, Topham DJ, D’Costa S, Cardin RD, Marion TN, Myers LK, Doherty PC (2000) Analysis of the virus-specific and nonspecific B cell response to a persistent B-lymphotropic gammaherpesvirus. J Immunol 164:1820–1828

    PubMed  CAS  Google Scholar 

  • Shakib F (1990). The human IgG subclasses: molecular analysis of structure, function and regulation. Pergamon Press, Oxford.

    Google Scholar 

  • Shokat KM, Goodnow CC (1995) Antigen-induced B-cell death and elimination during germinal-centre immune responses. Nature 375:334–338

    Article  PubMed  CAS  Google Scholar 

  • Siddiqui W, Tam L, Kramer K, Hui G, Case S, Yamaga K, Chang S, Chan E, Kan S (1987) Merozoite surface coat precursor protein completely protects Aotus monkeys against Plasmodium falciparum malaria. Proc Natl Acad Sci USA 84:3014–3018

    PubMed  CAS  Google Scholar 

  • Slifka MK, Ahmed R (1996) Long-term humoral immunity against viruses: revisiting the issue of plasma cell longevity. Trends Microbiol 4:394–400

    Article  PubMed  CAS  Google Scholar 

  • Slifka MK, Antia R, Whitmire JK, Ahmed R (1998) Humoral immunity due to long-lived plasma cells. Immunity 8:363–372

    Article  PubMed  CAS  Google Scholar 

  • Slifka MK, Matloubian M, Ahmed R (1995) Bone marrow is a major site of long-term antibody production after acute viral infection. J Virol 69:1895–1902

    PubMed  CAS  Google Scholar 

  • Smith T, Felger I, Tanner M, Beck HP (1999) Premunition in Plasmodium falciparum infection: insights from the epidemiology of multiple infections. Trans R Soc Trop Med Hyg 93 Suppl 1:59–64

    PubMed  Google Scholar 

  • Snow RW, Nahlen B, Palmer A, Donnelly CA, Gupta S, Marsh K (1998) Risk of severe malaria among African infants: direct evidence of clinical protection during early infancy. J Infect Dis 177:819–822

    Article  PubMed  CAS  Google Scholar 

  • Soares IS, da Cunha MG, Silva MN, Souza JM, Del Portillo HA, Rodrigues MM(1999a) Longevity of naturally acquired antibody responses to the N-and C-terminal regions of Plasmodium vivax merozoite surface protein 1. Am J Trop Med Hyg 60:357–363

    PubMed  CAS  Google Scholar 

  • Soares IS, Oliveira SG, Souza JM, Rodrigues MM (1999b) Antibody response to the N and C-terminal regions of the Plasmodium vivax Merozoite Surface Protein 1 in individuals living in an area of exclusive transmission of P. vivax malaria in the north of Brazil. Acta Trop 72:13–24

    PubMed  CAS  Google Scholar 

  • Staalso T, Hviid L(1998) The role of variant specific immunity in asymptomatic malaria infections: maintaining a fine balance. Parasitol Today 14:177

    Google Scholar 

  • Staalsoe T, Shulman CE, Bulmer JN, Kawuondo K, Marsh K, Hviid L (2004) Variant surface antigen-specific IgG and protection against clinical consequences of pregnancy-associated Plasmodium falciparum malaria. Lancet 363:283–289

    Article  PubMed  CAS  Google Scholar 

  • Stevenson MM, Tam MF (1993) Differential induction of helper T cell subsets during blood-stage Plasmodium chabaudi AS infection in resistant and susceptible mice. Clin Exp Immunol 92:77–83

    PubMed  CAS  Google Scholar 

  • Sze DM, Toellner KM, Garcia de Vinuesa C, Taylor DR, MacLennan IC (2000) Intrinsic constraint on plasmablast growth and extrinsic limits of plasma cell survival. J Exp Med 192:813–821

    Article  PubMed  CAS  Google Scholar 

  • Taylor RR, Egan A, McGuinness D, Jepson A, Adair R, Drakely C, Riley E (1996) Selective recognition of malaria antigens by human serum antibodies is not genetically determined but demonstrates some features of clonal imprinting. Int Immunol 8:905–915

    PubMed  CAS  Google Scholar 

  • Terrientes ZI, Kramer K, Herrera MA, Chang SP (1994) Naturally acquired antibodies against the major merozoite surface coat protein (MSP-1) of Plasmodium falciparum acquired by residents in an endemic area of Colombia.Mem Inst Oswaldo Cruz 89:55–61

    Article  PubMed  Google Scholar 

  • Tew JG, Mandel TE (1979) Prolonged antigen half-life in the lymphoid follicles of specifically immunized mice. Immunology 37:69–76

    PubMed  CAS  Google Scholar 

  • Tian JH, Miller LH, Kaslow DC, Ahlers J, Good MF, Alling DW, Berzofsky JA, Kumar S (1996) Genetic regulation of protective immune response in congenic strains of mice vaccinated with a subunit malaria vaccine. J Immunol 157:1176–1183

    PubMed  CAS  Google Scholar 

  • Tomoda T, Ogura H, Kurashige T (1992) The longevity of the immune response to filamentous hemagglutinin and pertussis toxin in patients with pertussis in a semiclosed community. J Infect Dis 166:908–910

    PubMed  CAS  Google Scholar 

  • Traggiai E, Puzone R, Lanzavecchia A (2003) Antigen dependent and independent mechanisms that sustain serum antibody levels. Vaccine 21 Suppl 2: S35–37

    Article  PubMed  CAS  Google Scholar 

  • Uzonna JE, Wei G, Yurkowski D, Bretscher P (2001) Immune elimination of Leishmania major in mice: implications for immune memory, vaccination, and reactivation disease. J Immunol 167:6967–6974

    PubMed  CAS  Google Scholar 

  • van der Heyde HC, Huszar D, Woodhouse C, Manning DD, Weidanz WP (1994) The resolution of acute malaria in a definitive model of B cell deficiency, the JHD mouse. J Immunol 152:4557–4562

    PubMed  Google Scholar 

  • van Druten H, van Knapen F, Reintjes A (1990) Epidemiologic implications of limited-duration seropositivity after toxoplasma infection. Am J Epidemiol 132:169–180

    PubMed  Google Scholar 

  • Vieira P, Rajewsky K (1990) Persistence of memory B cells in mice deprived of T cell help. Int Immunol 2:487–494

    PubMed  CAS  Google Scholar 

  • von der Weid T, Honarvar N, Langhorne J (1996) Gene-targeted mice lacking B cells are unable to eliminate a blood stage malaria infection. J Immunol 156:2510–2516

    PubMed  Google Scholar 

  • Vukovic P, Hogarth PM, Barnes N, Kaslow DC, Good MF (2000) Immunoglobulin G3 antibodies specific for the 19-kilodalton carboxyl-terminal fragment of Plasmodium yoelii merozoite surface protein 1 transfer protection to mice deficient in Fc-gammaRI receptors. Infect Immun 68:3019–3022

    Article  PubMed  CAS  Google Scholar 

  • Ward ES, Zhou J, Ghetie V, Ober RJ (2003) Evidence to support the cellular mechanism involved in serum IgG homeostasis in humans. Int Immunol 15:187–195

    Article  PubMed  CAS  Google Scholar 

  • Weidanz WP, Melancon-Kaplan J, Cavacini LA (1990) Cell-mediated immunity to the asexual blood stages of malarial parasites: animal models. Immunol Lett 25:87–95

    Article  PubMed  CAS  Google Scholar 

  • Xu H, Wipasa J, Yan H, Zeng M, Makobongo MO, Finkelman FD, Kelso A, Good MF (2002) The mechanism and significance of deletion of parasite-specific CD4(+) T cells in malaria infection. J Exp Med 195:881–892

    Article  PubMed  CAS  Google Scholar 

  • Zerboni L, Nader S, Aoki K, Arvin AM (1998) Analysis of the persistence of humoral and cellular immunity in children and adults immunized with varicella vaccine. J Infect Dis 177:1701–1704

    Article  PubMed  CAS  Google Scholar 

  • Zevering Y, Khamboonruang C, Rungruengthanakit K, Tungviboonchai L, Ruengpipattanapan J, Bathurst I, Barr P, Good MF (1994) Life-spans of human T-cell responses to determinants from the circumsporozoite proteins of Plasmodium falciparum and Plasmodium vivax. Proc Natl Acad Sci USA 91:6118–6122

    PubMed  CAS  Google Scholar 

  • Zinkernagel RM (2002) On differences between immunity and immunological memory. Curr Opin Immunol 14:523–536

    Article  PubMed  CAS  Google Scholar 

  • Zinkernagel RM, Hengartner H (2001) Regulation of the immune response by antigen. Science 293:251–253

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2005 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Achtman, A.H., Bull, P.C., Stephens, R., Langhorne, J. (2005). Longevity of the Immune Response and Memory to Blood-Stage Malaria Infection. In: Langhorne, J. (eds) Immunology and Immunopathogenesis of Malaria. Current Topics in Microbiology and Immunology, vol 297. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-29967-X_3

Download citation

Publish with us

Policies and ethics