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PMID: 1719084 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Identification and characterization of a T cell-inducing epitope of bovine ribonuclease that can be restricted by multiple class II molecules.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 147 ·No. 11 ·1991-12-01 ·Pages 3672-8

Chen JS, Lorenz RG, Goldberg J, Allen PM

Abstract

An immunodominant epitope of bovine RNase restricted by I-Ek molecules was identified using a T cell hybridoma recognizing RNase. This epitope was localized to the peptide RNase(90-105). Single conservative amino acid substitutions were made at each of the positions 94 through 105. It was found that only at one position, Asn-103, were conservative substitutions not allowed. This residue was shown to be the critical residue in determining T cell specificity. The ability of RNase(90-105) and the well-defined T cell epitope, HEL(46-61) to stimulate mouse strains expressing different independent H-2 haplotypes was examined using a T cell proliferation assay. The response to HEL(46-61) was completely restricted to mice expressing an I-Ak molecule. In striking contrast, 6 of 10 different mouse strains, H-2b,f,k,q,s,u, mounted vigorous T cell responses to RNase(90-105). The response was restricted to both I-A and I-E molecules, including I-Ab, I-Af, I-Ek, I-Aq, and I-As. H-2d mice were nonresponders to RNase(90-105), which was shown to be due to the failure of RNase(90-105) to bind to I-Ad molecules. A variant RNase(90-105) peptide was generated, containing an I-Ad binding motif, that could bind to I-Ad molecules. Despite its ability to bind, this variant peptide was not able to stimulate a response in H-2d mice. This result demonstrates that the ability of a peptide to bind to an Ia molecule is necessary but not always sufficient for a response to occur. Thus, in contrast to the highly restricted HEL(46-61) determinant, the RNase(90-105) determinant is permissive in its binding to Ia molecules. These results show that in the universe of T cell inducing epitopes contains both highly restricted and broadly restricted epitopes are found.

MeSH Terms
Amino Acid Sequence Animals Antigen-Presenting Cells/immunology Cattle Epitopes Histocompatibility Antigens Class II/immunology Lymphocyte Activation Mice Mice, Inbred Strains Molecular Sequence Data Ribonucleases/immunology Structure-Activity Relationship T-Lymphocytes/immunology
Chemicals
Epitopes Histocompatibility Antigens Class II I-E-antigen Ribonucleases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Chen J S
Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110.
Lorenz R G
Goldberg J
Allen P M
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1991-12-01
Pages
3672-8
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI-24157 · United States
NIAID NIH HHS · AI-28716 · United States
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