These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
199 related articles for article (PubMed ID: 7534415)
1. Identification of a major I-Ek-restricted determinant of hen egg lysozyme: limitations of lymph node proliferation studies in defining immunodominance and crypticity. Viner NJ; Nelson CA; Unanue ER Proc Natl Acad Sci U S A; 1995 Mar; 92(6):2214-8. PubMed ID: 7534415 [TBL] [Abstract][Full Text] [Related]
2. Antigen presentation by dendritic cells focuses T cell responses against immunodominant peptides: studies in the hen egg-white lysozyme (HEL) model. Gapin L; Bravo de Alba Y; Casrouge A; Cabaniols JP; Kourilsky P; Kanellopoulos J J Immunol; 1998 Feb; 160(4):1555-64. PubMed ID: 9469410 [TBL] [Abstract][Full Text] [Related]
3. Analysis of T cell reactivities to phosphorylcholine-conjugated hen egg lysozyme in C57BL/6 mice: hapten-conjugate specificity reflects an altered expression of a major carrier epitope. Jang YS; Lim KH; Kim BS Eur J Immunol; 1991 May; 21(5):1303-10. PubMed ID: 1709872 [TBL] [Abstract][Full Text] [Related]
4. Processing of endogenously synthesized hen egg-white lysozyme retained in the endoplasmic reticulum or in secretory form gives rise to a similar but not identical set of epitopes recognized by class II-restricted T cells. Adorini L; Guéry JC; Fuchs S; Ortiz-Navarrete V; Hämmerling GJ; Momburg F J Immunol; 1993 Oct; 151(7):3576-86. PubMed ID: 7690807 [TBL] [Abstract][Full Text] [Related]
5. Constraints in antigen processing result in unresponsiveness to a T cell epitope of hen egg lysozyme in C57BL/6 mice. Kim BS; Jang YS Eur J Immunol; 1992 Mar; 22(3):775-82. PubMed ID: 1372259 [TBL] [Abstract][Full Text] [Related]
6. Cytosolic targeting of hen egg lysozyme gives rise to a short-lived protein presented by class I but not class II major histocompatibility complex molecules. Calin-Laurens V; Forquet F; Mottez E; Kanellopoulos J; Godeau F; Kourilsky P; Gerlier D; Rabourdin-Combe C Eur J Immunol; 1991 Mar; 21(3):761-9. PubMed ID: 2009914 [TBL] [Abstract][Full Text] [Related]
7. Co-dominant restriction by a mixed-haplotype I-A molecule (alpha k beta b) for the lysozyme peptide 52-61 in H-2k x H-2b F1 mice. Moreno J; Adorini L; Hämmerling GJ J Immunol; 1990 May; 144(9):3296-304. PubMed ID: 1970351 [TBL] [Abstract][Full Text] [Related]
8. T cell epitope recognition involved in the low-responsiveness to a region of hen egg lysozyme (46-61) in C57BL/6 mice. Jang YS; Mikszta JA; Kim BS Mol Immunol; 1994 Aug; 31(11):803-12. PubMed ID: 7519304 [TBL] [Abstract][Full Text] [Related]
9. Comparison of structural requirements for interaction of the same peptide with I-Ek and I-Ed molecules in the activation of MHC class II-restricted T cells. Leighton J; Sette A; Sidney J; Appella E; Ehrhardt C; Fuchs S; Adorini L J Immunol; 1991 Jul; 147(1):198-204. PubMed ID: 1711074 [TBL] [Abstract][Full Text] [Related]
10. DM determines the cryptic and immunodominant fate of T cell epitopes. Nanda NK; Sant AJ J Exp Med; 2000 Sep; 192(6):781-8. PubMed ID: 10993909 [TBL] [Abstract][Full Text] [Related]
12. Cathepsin D, but not cathepsin B, releases T cell stimulatory fragments from lysozyme that are functional in the context of multiple murine class II MHC molecules. van Noort JM; Jacobs MJ Eur J Immunol; 1994 Sep; 24(9):2175-80. PubMed ID: 8088334 [TBL] [Abstract][Full Text] [Related]
13. Interaction of an immunodominant epitope with Ia molecules in T-cell activation. Adorini L; Sette A; Buus S; Grey HM; Darsley M; Lehmann PV; Doria G; Nagy ZA; Appella E Proc Natl Acad Sci U S A; 1988 Jul; 85(14):5181-5. PubMed ID: 2455895 [TBL] [Abstract][Full Text] [Related]
14. Increasing the frequency of T-cell precursors specific for a cryptic epitope of hen-egg lysozyme converts it to an immunodominant epitope. Thatcher TH; O'Brien DP; Altuwaijri S; Barth RK Immunology; 2000 Feb; 99(2):235-42. PubMed ID: 10692042 [TBL] [Abstract][Full Text] [Related]
15. Modification of the inhibitory amino acid for epitope peptide binding onto major histocompatibility complex class II molecules enhances immunogenicity of the antigen. Chang SH; Kim J; Lee KY; Kim HJ; Chung YJ; Park CU; Kim BS; Jang YS Scand J Immunol; 2004 Feb; 59(2):123-32. PubMed ID: 14871288 [TBL] [Abstract][Full Text] [Related]
16. Processing and reactivity of T cell epitopes containing two cysteine residues from hen egg-white lysozyme (HEL74-90). Kang HK; Mikszta JA; Deng H; Sercarz EE; Jensen PE; Kim BS J Immunol; 2000 Feb; 164(4):1775-82. PubMed ID: 10657624 [TBL] [Abstract][Full Text] [Related]
17. Selective immunosuppression by administration of major histocompatibility complex (MHC) class II-binding peptides. I. Evidence for in vivo MHC blockade preventing T cell activation. Guéry JC; Sette A; Leighton J; Dragomir A; Adorini L J Exp Med; 1992 May; 175(5):1345-52. PubMed ID: 1569402 [TBL] [Abstract][Full Text] [Related]
18. Threshold detection of self-antigen/MHC class II complexes formed in vivo: constitutive presentation of an immunodominant epitope of hen egg lysozyme (HEL) in HEL-transgenic mice. Kanost D; Basten A; McCluskey J Int Immunol; 1993 Aug; 5(8):893-902. PubMed ID: 8398984 [TBL] [Abstract][Full Text] [Related]
19. Complexes generated by the binding of free peptides to class II MHC molecules are antigenically diverse compared with those generated by intracellular processing. Viner NJ; Nelson CA; Deck B; Unanue ER J Immunol; 1996 Apr; 156(7):2365-8. PubMed ID: 8786292 [TBL] [Abstract][Full Text] [Related]
20. Hindrance of binding to class II major histocompatibility complex molecules by a single amino acid residue contiguous to a determinant leads to crypticity of the determinant as well as lack of response to the protein antigen. Grewal IS; Moudgil KD; Sercarz EE Proc Natl Acad Sci U S A; 1995 Feb; 92(5):1779-83. PubMed ID: 7533299 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]