Administration of PLP139-151 primes T cells distinct from those spontaneously responsive in vitro to this antigen

We examined the TCR repertoire used by naive SJL mice in their in vitro spontaneous response to proteolipid protein (PLP) 139-151 by V beta-J beta spectratyping and compared it to that used after immunization with the peptide. T cells from immunized mice use the public rearrangement V beta 10-J beta 1.1, but naive mice do not; in contrast, TCR CDR3-beta rearrangements of V beta 18-J beta 1.2 and V beta 19-J beta 1.2 consistently are associated with the spontaneous response. T cells involved in spontaneous and induced responses can each recognize PLP139-151 presented in vivo, but its s.c. administration has different consequences for the two repertoires. Four days after immunization, T cells associated with spontaneous responsiveness appear in the draining lymph nodes but disappear by day 10 and never appear elsewhere. Simultaneously, V beta 10-J beta 1.1 T cells are likewise activated in the lymph nodes by day 4 and spread to the spleen by day 10. Eight- to 10-wk-old naive mice use a narrower repertoire or TCRs than do immunized age-matched mice. Induced V beta 10-J beta 1.1 T cells home to the CNS during experimental autoimmune encephalomyelitis, whereas we failed to detect V beta 18-J beta 1.2 and V beta 19-J beta 1.2 TCR rearrangements in the CNS. Thus, we observe that administration of PLP139-151 primes a T cell repertoire distinct from the one responsible for spontaneous responsiveness. This immunized repertoire substitutes for the naive one and becomes dominant at the time of disease onset.