Hm. Wolf et al., Long-term decrease of CD4(+)CD45RA(+) T cells and impaired primary immune response after post-traumatic splenectomy, BR J HAEM, 107(1), 1999, pp. 55-68
Congenital or acquired absence of the spleen and functional hyposplenism ar
e associated with abnormalities of host defence such as an increased suscep
tibility to infection with encapsulated bacteria. The effects of the lack o
f the spleen on cell-mediated immunity are largely unknown. In the present
study we have investigated peripheral blood lymphocyte subpopulations in he
althy adults who had undergone splenectomy because of severe abdominal trau
ma >4 years before the study. The results show a significant reduction in t
he percentage of CD4(+) T cells due to a selective and long-term decrease i
n the percentage of CD4(+)CD45RA(+) lymphocytes, the CD4(+) T-cell subset m
ainly involved in primary immune responses to newly encountered antigens. L
evels of the reciprocal CD45RO(+)CD4(+) T-cell subset were comparable betwe
en splenectomized and control individuals, as were lymphoproliferative resp
onses and IFN-gamma production to recall antigens. Decreased levels of CD4(
+)CD45RA(+) cells were accompanied by an impairment in primary immune respo
nsiveness, as assessed by investigating T-cell proliferation to stimulation
with keyhole limpet haemocyanin and by measuring antibody responses follow
ing primary immunization with a clinically relevant T-dependent antigen, he
patitis A vaccine, in vivo. These findings suggest a possible role of the s
pleen in the generation, maintenance and/or differentiation of naive, unpri
med T cells or their precursors, which might have a possible functional rel
evance for primary immune responses following splenectomy.