BIOM20001 Lecture Notes - Lecture 54: Passive Immunity, Mhc Class I, Mhc Class Ii

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6 Oct 2018
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Heavy and light chain gene rearrangements in b cells. Are result of random somatic gene rearrangements (d-j, v-dj, v-j) Rearranged genes give rise to unique heavy and light chain protein sequences. Recombinations of v, d and j genes are facilitated by recombinase enzymes: Recombinase activating genes (rag"s) terminal deoxynucleotide transferases (tdt) and exonucleases. Defects in above genes result in a block in recom and an absence of circulating b cells. Since b cell that can"t produce pre-b cell receptor (can"t rearrange genes will be deleted) Need many antibody specificities (e. g. 1011 specificities in humans) This diversity generated by ig rearrangement and junctional events, e. g. ig gene rearrangements are random. Before leaving the bone marrow those that bind self molecules in the bone marrow are deleted. B cells that survive this process migrate to the circulation were they now express both igd and. Further diversity due to somatic hypermutation introduced in secondary lymphoid tissue after antigen binding.

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