T-CELL PEPTIDE OF A SELF-PROTEIN ELICITS AUTOANTIBODY TO THE PROTEIN ANTIGEN - IMPLICATIONS FOR SPECIFICITY AND PATHOGENETIC ROLE OF ANTIBODY IN AUTOIMMUNITY
Yh. Lou et Ksk. Tung, T-CELL PEPTIDE OF A SELF-PROTEIN ELICITS AUTOANTIBODY TO THE PROTEIN ANTIGEN - IMPLICATIONS FOR SPECIFICITY AND PATHOGENETIC ROLE OF ANTIBODY IN AUTOIMMUNITY, The Journal of immunology, 151(10), 1993, pp. 5790-5799
A 13-mer peptide of the ZP3 glycoprotein from mouse zona pellucida has
a T cell epitope that induces autoimmune oophoritis and a B cell epit
ope that reacts with antibody to murine ZP3. When the B cell epitope w
as partially truncated, the ZP3 peptides no longer induced antibody to
the B cell epitope, but unexpectedly they elicited antibody to the zo
na pellucida. These autoantibodies were of IgG class, detected in sera
and bound to the ovarian zona pellucida. That an exclusive T cell pep
tide of murine ZP3, without coinjection of the whole ZP3 protein, elic
ited autoantibodies against ZP3 outside the T cell peptide was confirm
ed as follows. First, the ZP3 T cell peptide did not contain additiona
l B cell epitopes that cross-reacted with native ZP3. Second, endogeno
us ovarian Ag were required because autoantibodies were not detected i
n ovariectomized mice immunized with ZP3 peptides lacking the B epitop
e. This autoantibody amplification phenomenon demonstrates conclusivel
y that 1) self-reactive B cells for ovarian autoantigens respond to en
dogenous ovarian Ag in vivo after activation of ZP3-specific Th cells
and 2) serum antibody in an autoimmune disease need not mirror the imm
unogen that initiates the disease process. Nonetheless, the autoantibo
dies bound to the zona pellucida in vivo and are potentially important
in disease pathogenesis.