Cellular immune reactivity within the CNS

H Wekerle, C Linington, H Lassmann… - Trends in …, 1986 - cell.com
H Wekerle, C Linington, H Lassmann, R Meyermann
Trends in neurosciences, 1986cell.com
Fig. 1. Antigen recognition by T lymphocyte subsets. T lymphocytes recognize antigen only
when it is presented on the membrane of suitable antigen presenting cells (APC). T cells of
one major subset (CD4) are characterized by the human monoclonal marker T4 (mouse
L3T4, rat W3/25) and contain the majority of the helper T lymphocytes; they recognize their
antigen (0) only in association with class H histo-'compatibility molecules (la determinants)
on the A PC. T cells of the complementary subset (C Dg) defined by the marker T8 (mouse L …
Fig. 1. Antigen recognition by T lymphocyte subsets. T lymphocytes recognize antigen only when it is presented on the membrane of suitable antigen presenting cells (APC). T cells of one major subset (CD4) are characterized by the human monoclonal marker T4 (mouse L3T4, rat W3/25) and contain the majority of the helper T lymphocytes; they recognize their antigen (0) only in association with class H histo-'compatibility molecules (la determinants) on the A PC. T cells of the complementary subset (C Dg) defined by the marker T8 (mouse L yt 2, rat oxg), contain suppressor and killer cells and recognize antigen in the context of class I histocompatibility antigens. These histocompatibility antigens are polymorphic cell surface glycoproteins, Following recognition of the antigen, originally resting T cells are activated. Activation involves a drastic increase in cellular metabolism, induction of T cell mediators and receptors for growth factors, and rapid cell division, leading to the formation of large lymphoblasts.
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