I now have excellent source material. The Vasudevan textbook is not in the library, but the concept is clearly and authoritatively explained in Robbins & Cotran Pathologic Basis of Disease and Roitt's Essential Immunology. I can now write a precise 2-mark reasoning answer aligned with standard biochemistry/immunology teaching as covered in Vasudevan.
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Central tolerance - Clonal deletion (Negative selection): During the maturation of lymphocytes, immature B cells and T cells whose antigen receptors happen to recognize self-antigens (the body's own proteins) are identified and eliminated by apoptosis in the primary lymphoid organs - T cells in the thymus and B cells in the bone marrow. This process of physically destroying self-reactive clones before they can reach the periphery is called clonal deletion. The protein AIRE (autoimmune regulator) expressed in the thymus plays a key role by displaying a wide range of tissue-specific self-antigens to developing T cells, ensuring that cells reactive to them are deleted.
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Peripheral tolerance - Clonal anergy: Any self-reactive lymphocytes that escape central deletion and enter peripheral tissues are rendered functionally unresponsive (anergic) in the absence of proper co-stimulatory signals, preventing them from mounting an immune response against self-proteins.
Note: A breakdown of self-tolerance leads to autoimmune diseases, where the body does begin producing antibodies against its own tissues (e.g., Rheumatoid Arthritis, SLE, Graves' disease).