Abstract
A series of cells and antibody proteins make up a critically important system of immunity. This immunological system, when functioning adequately, protects us against infections by bacterial, parasitic, viral and fungal agents, and even against the growth of cancer cells. When the system does not function normally, we are plagued by a wide array of diseases. One of the fundamental questions in the field of immunology is how the immune system recognises up to 100 million substances as foreign, yet normally does not direct its attack against the tissues of the individual. Over the past few years there have been enormous advances in our understanding of how the human immune system is regulated. A number of these insights have emerged from the study of neoplasms of the B cell/plasma cell and of the T cell series. For example, the recognition that paraproteins derived from patients with multiple myeloma represent homogeneous immunoglobulins was an indispensable step in understanding the structural and functional aspects of immunoglobulin molecules. In this chapter I shall focus on studies of leukaemic B and T lymphocytes which were directed towards defining the molecular events and cellular interactions that control immunoglobulin synthesis. In the first section I shall discuss studies applying the techniques of molecular biology to lymphoid cells which were directed towards defining the early events in the differentiation of stem cells into B cells.
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Waldmann, T.A. (1984). In vitro and in vivo regulation of immunoglobulin synthesis. In: Mariani, G. (eds) Pathophysiology of Plasma Protein Metabolism. Palgrave, London. https://doi.org/10.1007/978-1-349-06680-3_7
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DOI: https://doi.org/10.1007/978-1-349-06680-3_7
Publisher Name: Palgrave, London
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