Increased Mucosal IL-22 Production of an IL-10RA Mutation Patient Following Anakinra Treatment Suggests Further Mechanism for Mucosal Healing
KeywordsHematopoietic Stem Cell Transplantation Anakinra Mucosal Healing Hidradenitis Suppurativa Enterocutaneous Fistula
To the Editor:
IL10 is an immunoregulatory cytokine that has a central role in the maintenance of intestinal mucosal homeostasis and prevention of colitis . Loss-of-function mutations in IL10, IL10RA, or IL10RB cause severe intestinal inflammation and perianal disease that presents in the first months of life and is refractory to conventional immunosuppressive medications such as steroids, anti-TNFα antibodies, and immunomodulators . The definitive treatment for IL10R deficiency is an allogeneic hematopoietic stem cell transplantation (HSCT) to reconstitute IL10 signaling, if a suitable donor is available. Unfortunately, the clinical condition of many of these patients is not amenable to transplant at the time of their diagnosis. As such, a therapeutic bridge is needed to prepare them for transplant.
We have recently shown that IL1β is highly upregulated in IL10R deficiency , and blocking IL1 attenuated colitis in an IL10R-deficient mouse model. Thus, we elected to treat two patients with medical-refractory severe inflammatory bowel disease (IBD) secondary to IL10R deficiency with anakinra, an IL1 receptor antagonist. In both cases, high dose anakinra therapy (10–12 mg/kg/day) led to marked clinical, endoscopic, and histological improvement within a few weeks . To date, this is the first report of treatment that suppressed the hyperactive immune response in the gut of these patients.
To further understand the mechanism of anakinra treatment in the IL10R-deficient patient, we compared the frequency of IL22-producing lymphocytes in lamina propria mononuclear cells (LPMC) isolated from his terminal ileum biopsy samples taken pre- and post-anakinra treatment. IL22-producing lymphocytes were our primary targets because of their known role in healing of intestinal inflammation. In the lineage negative compartment, we did not find IL22-producing innate lymphoid cell group 3 (ILC3). However, the frequency of IL22-producing lymphocytes among lineage (+) CD45 (+) LPMC greatly increased from 2.17% pre-anakinra to 50.9% post-anakinra (Fig. 1b). Analysis of an additional ileal biopsy 3 months later demonstrated that the number further increased to 53.9% among lineage (+) CD45 (+) LPMC (Fig. 1b). Furthermore, H&E staining of this additional biopsy showed resolution of the severely inflamed ileal region 5 cm above the ileostomy (Fig. 1a). The remaining 5 cm with associated enterocutaous fistulae remained inflamed. In addition, as mentioned in our recent publication, the inflammatory changes in the skin adjacent to the patient’s ileostomy and fistulae also resolved. Overall, our data suggest that anakinra-induced IL22 production may have a role in mucosal healing in this IL10R-deficient patient.
During a recent clinical trial among hidradenitis suppurativa patients, Vassiliki et al. observed significantly increased production of IL22 by peripheral blood mononuclear cells (PBMC) following anakinra therapy and concluded that the increased IL22 might contribute to an improved epithelial cell defense . Based on these observations, we decided to assess IL22 production in the LPMC compartment of our sporadic adult Crohn’s disease population (Supplementary Table. 1). We detected a trend towards reduction of the IL22-producing lymphocytes (p = 0.07) among Lineage (+) CD45 (+) LPMC in the inflamed tissue (2.89%, n = 9) compared to unaffected tissue (5.75%, n = 3) (Fig. 1c). This result complements another report that IL22-producing CD4+ cells were depleted in active inflamed lesions of ulcerative colitis (UC) patients .
The deficiency of IL22-producing lymphocytes in the inflamed gut and the fact that its recovery coincided with improved intestinal inflammation suggest a protective role of this population in the gastrointestinal tract and that it might serve as a surrogate marker of mucosal healing. IL22 is a member of the IL10 family of cytokines. It directly binds to the heterodimeric receptor IL22Rα1-IL10Rβ on non-hematopoietic cells, especially on epithelial cells. The binding of IL22 promotes epithelial cell proliferation; secretion of antimicrobial peptides such as RegIIIβ, RegIIIγ, S108a, and S109a; and mucus production as well as fucosylation. Specifically, IL22 stimulation leads to the activation of signal transducer and activator of transcription 3 (STAT3) in epithelial cells, which contributes to tissue repair after injury. Finally, it is important to mention that this patient is an IL10RA mutation and his IL10RB is intact. This guarantees the responsiveness of epithelial cell to the increased IL22 signaling. Response to anakinra in IL10RB-deficient patients might be less effective but warrants further evaluation.
We subsequently assessed whether the frequency of circulating IL22-producing lymphocytes was altered in our IL10R-deficient patient, when compared to a Crohn’s disease cohort and normal controls. Indeed, we observed a significant increase in blood-borne TH22 and TH17 cells, both single producers and IL22/IFNγ, IL17A/IFNγ double producers, in the patient, as well as in Crohn’s disease subjects (Fig. 1d and Supplementary Fig. 1). It is important to note that the IL10R-deficient patient was analyzed after starting anakinra therapy, which we know decreased mucosal IL17 in both treated patients and might also influence circulating TH17 cells .
In conclusion, we present a case of a patient with severe IBD due to an IL10RA mutation who demonstrated a dramatic response to anakinra therapy. This intervention led to mucosal healing accompanied by increased frequency of IL22-producing lymphocytes in the lamina propria of the terminal ileum. The increase in IL22, which promoted tissue repair, might have had an important role in the recovery of this patient and suggests an additional important mechanistic mode of action of anakinra in the gut.
This study was approved by the IRBs at the University of Florida and Boston Children’s hospital. We thank Dr. Xiuli Liu from the Department of Pathology, University of Florida Health for providing the histology pictures.
S.C.G is supported by Gatorade funding from University of Florida and the Mary Parker Foundation. S.B.S is supported by NIH Grants HL59561, DK034854, and AI50950, the Helmsley Charitable Trust, and the Wolpow Family Chair in IBD Treatment and Research.
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Conflict of Interest
The authors have no conflicts of interest related to this project. Sarah Glover, DO is a consultant for AbbVie, Janssen, and Takeda. Sarah Glover, DO has received grant support from AbbVie, Bristol Myers Squibb, Celgene, Gilead, Janssen, Genentech, Millennium, Pfizer, Receptos, Takeda, and UCB.
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