N. Fabien et al., Autoantibodies directed against the ribosomal P proteins are not only directed against a common epitope of the P0, P1 and P2 proteins, J AUTOIMMUN, 13(1), 1999, pp. 103-110
The autoantibodies (aAbs) directed against the ribosomal P proteins (RPP aA
bs) are known to react mainly against epitopes localized within the common
C-terminal sequence of the three acidic ribosomal P proteins, P0, P1 and P2
. In order to investigate the opportunity to select short recombinant pepti
des of this common C-terminal sequence to detect the RPP-aAbs, the location
of the epitopes recognized by ribosomal proteins (RP) aAb(+) sera of syste
mic lupus erythematosus patients (SLE) was investigated. Immunoblotting and
ELISA techniques using extracted or recombinant, entire or cleaved RPP sho
wed that 55% of the RP aAbs were directed against the three ribosomal PO, P
1, and P2 proteins. The epitopes recognized by the RPP aAbs are located not
only within the C-terminal sequence common to the three proteins but also
within the N-terminal sequence of the P2 or P1 protein. The other RP aAbs s
era (45%) did not react with all three proteins but with some of them, and
showed the following pattern: P0(+) P1(+); P1(+); P2(+); P0(+) and P1(+) Th
ey recognized epitopes located in the region of the C-terminal sequence of
the protein but not common to the three proteins. In addition two out of th
e six monoclonal Abs produced by immunization of mice using the P1 protein
did not react with the peptide N-65 or N-71 of the P2 protein or with the C
-terminal sequence of the three proteins. In conclusion this study showed t
hat the RPP aAb in SLE patients are not only directed against epitopes with
in the C-terminal sequence shared by the three acidic ribosomal P proteins.
In view of these data it seems necessary to be cautious in using only a C-
terminal peptide of ribosomal P proteins in tests performed to detect RPP a
Ab in human sera. (C) 1999 Academic Press.