F. Batliwalla et al., OLIGOCLONALITY OF CD8-CELLS IN HEALTH AND DISEASE - AGING, INFECTION,OR IMMUNE REGULATION( T), Human immunology, 48(1-2), 1996, pp. 68-76
Oligoclonality of the CD8+ T cell subset is a common and characteristi
c feature of the normal human peripheral T cell repertoire. These clon
ally expanded populations are predominantly found in a CD57+ or CD28-
CD8+ T cell subset. While CD8 oligoclonality is somewhat more common i
n the older age group, it is also very prevalent in young to middle-ag
ed adults. Recent experiments have also demonstrated that the clonally
expanded populations may actually occur in two distinct subpopulation
s of CD8+ CD28- cells, distinguished by the expression of the CD57 sur
face marker, A major difficulty with studies involving CD8+ CD28- CD57
+ T cells is their relative lack of proliferative capacity. We have re
cently investigated the possibility that this phenotype may be due to
a state of ''replicative senescence'' in some cases. In this regard, w
e have demonstrated that the telomere lengths of CD8+ CD28- T cells ar
e generally shorter than that of their CD8+ CD28+ counterparts, consis
tent with a distinct replicative history for the CD8+ CD28- population
. Additional studies of the normal biology of clonally expanded CD8+ T
cells are likely to yield important insights into immune function in
health and disease.