Repertoire analysis and new pathogenic epitopes of IRBP in C57BL/6 (H-2 b) and B10.RIII (H-2 r) mice

Lizette M. Cortes, Mary J. Mattapallil, Phyllis B. Silver, Larry A. Donoso, Gregory I. Liou, Wei Zhu, Chi Chao Chan, Rachel R. Caspi

Research output: Contribution to journalArticle

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Abstract

Purpose. Interphotoreceptor retinoid binding protein (IRBP) is the major uveitogenic retinal antigen eliciting experimental autoimmune uveoretinitis (EAU) in mice. The most frequently used mouse strains are B10.RIII and C57BL/6, but to date only one uveitogenic epitope for each has been identified. The purpose of this study was to identify and characterize additional uveitogenic epitopes in B10.RIII and C57BL/6 mice and to compare epitope recognition in wild-type versus IRBP-defi- cient mice on both backgrounds. Methods. Mice were immunized with IRBP. Spleen cells were stimulated in culture with overlapping peptides representing the entire IRBP molecule, and lymphocyte proliferative responses were measured. Peptides determined to be immuno- dominant were used to immunize mice for EAU. Cytokine profile and proliferation of the CD4 versus CD8 subsets were analyzed for the most pathogenic peptides. Results. Two new major pathogenic epitopes were identified in WT C57BL/6 mice, residues 461-480 and 651-670. These epitopes induced EAU of severity similar to that induced by the previously known peptide, 1-20. Several other peptides elicited mild disease with lower incidence. Some peptides elicited EAU only in WT recipients of IRBP KO splenocytes. In the B10.RIII strain, two major new uveito- genic peptides were identified, 171-190 and 541-560, and several others elicited moderate disease. Unlike in C57BL/6 mice, adoptive transfer of WT B10.RIII with IRBP KO spleno- cytes did not reveal additional uveitogenic epitopes. Both CD4 and CD8 lymphocyte subsets proliferated to pathogenic peptides. Conclusions. Several new pathogenic peptides of IRBP were identified in C57BL/6 and B10.RIII mice. Differences in epitope recognition between WT and IRBP KO mice were observed in C57BL/6 mice, but not in B10.RIII mice, suggesting more extensive culling of the repertoire in C57BL/6 mice by endo- genously expressed IRBP.

Original languageEnglish (US)
Pages (from-to)1946-1956
Number of pages11
JournalInvestigative Ophthalmology and Visual Science
Volume49
Issue number5
DOIs
StatePublished - Apr 1 2008

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Epitopes
Peptides
Inbred C57BL Mouse
interstitial retinol-binding protein
Adoptive Transfer
Lymphocyte Subsets
Spleen
Lymphocytes
Cytokines
Antigens
Incidence

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems
  • Cellular and Molecular Neuroscience

Cite this

Cortes, L. M., Mattapallil, M. J., Silver, P. B., Donoso, L. A., Liou, G. I., Zhu, W., ... Caspi, R. R. (2008). Repertoire analysis and new pathogenic epitopes of IRBP in C57BL/6 (H-2 b) and B10.RIII (H-2 r) mice. Investigative Ophthalmology and Visual Science, 49(5), 1946-1956. https://doi.org/10.1167/iovs.07-0868

Repertoire analysis and new pathogenic epitopes of IRBP in C57BL/6 (H-2 b) and B10.RIII (H-2 r) mice. / Cortes, Lizette M.; Mattapallil, Mary J.; Silver, Phyllis B.; Donoso, Larry A.; Liou, Gregory I.; Zhu, Wei; Chan, Chi Chao; Caspi, Rachel R.

In: Investigative Ophthalmology and Visual Science, Vol. 49, No. 5, 01.04.2008, p. 1946-1956.

Research output: Contribution to journalArticle

Cortes, LM, Mattapallil, MJ, Silver, PB, Donoso, LA, Liou, GI, Zhu, W, Chan, CC & Caspi, RR 2008, 'Repertoire analysis and new pathogenic epitopes of IRBP in C57BL/6 (H-2 b) and B10.RIII (H-2 r) mice', Investigative Ophthalmology and Visual Science, vol. 49, no. 5, pp. 1946-1956. https://doi.org/10.1167/iovs.07-0868
Cortes, Lizette M. ; Mattapallil, Mary J. ; Silver, Phyllis B. ; Donoso, Larry A. ; Liou, Gregory I. ; Zhu, Wei ; Chan, Chi Chao ; Caspi, Rachel R. / Repertoire analysis and new pathogenic epitopes of IRBP in C57BL/6 (H-2 b) and B10.RIII (H-2 r) mice. In: Investigative Ophthalmology and Visual Science. 2008 ; Vol. 49, No. 5. pp. 1946-1956.
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abstract = "Purpose. Interphotoreceptor retinoid binding protein (IRBP) is the major uveitogenic retinal antigen eliciting experimental autoimmune uveoretinitis (EAU) in mice. The most frequently used mouse strains are B10.RIII and C57BL/6, but to date only one uveitogenic epitope for each has been identified. The purpose of this study was to identify and characterize additional uveitogenic epitopes in B10.RIII and C57BL/6 mice and to compare epitope recognition in wild-type versus IRBP-defi- cient mice on both backgrounds. Methods. Mice were immunized with IRBP. Spleen cells were stimulated in culture with overlapping peptides representing the entire IRBP molecule, and lymphocyte proliferative responses were measured. Peptides determined to be immuno- dominant were used to immunize mice for EAU. Cytokine profile and proliferation of the CD4 versus CD8 subsets were analyzed for the most pathogenic peptides. Results. Two new major pathogenic epitopes were identified in WT C57BL/6 mice, residues 461-480 and 651-670. These epitopes induced EAU of severity similar to that induced by the previously known peptide, 1-20. Several other peptides elicited mild disease with lower incidence. Some peptides elicited EAU only in WT recipients of IRBP KO splenocytes. In the B10.RIII strain, two major new uveito- genic peptides were identified, 171-190 and 541-560, and several others elicited moderate disease. Unlike in C57BL/6 mice, adoptive transfer of WT B10.RIII with IRBP KO spleno- cytes did not reveal additional uveitogenic epitopes. Both CD4 and CD8 lymphocyte subsets proliferated to pathogenic peptides. Conclusions. Several new pathogenic peptides of IRBP were identified in C57BL/6 and B10.RIII mice. Differences in epitope recognition between WT and IRBP KO mice were observed in C57BL/6 mice, but not in B10.RIII mice, suggesting more extensive culling of the repertoire in C57BL/6 mice by endo- genously expressed IRBP.",
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T1 - Repertoire analysis and new pathogenic epitopes of IRBP in C57BL/6 (H-2 b) and B10.RIII (H-2 r) mice

AU - Cortes, Lizette M.

AU - Mattapallil, Mary J.

AU - Silver, Phyllis B.

AU - Donoso, Larry A.

AU - Liou, Gregory I.

AU - Zhu, Wei

AU - Chan, Chi Chao

AU - Caspi, Rachel R.

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N2 - Purpose. Interphotoreceptor retinoid binding protein (IRBP) is the major uveitogenic retinal antigen eliciting experimental autoimmune uveoretinitis (EAU) in mice. The most frequently used mouse strains are B10.RIII and C57BL/6, but to date only one uveitogenic epitope for each has been identified. The purpose of this study was to identify and characterize additional uveitogenic epitopes in B10.RIII and C57BL/6 mice and to compare epitope recognition in wild-type versus IRBP-defi- cient mice on both backgrounds. Methods. Mice were immunized with IRBP. Spleen cells were stimulated in culture with overlapping peptides representing the entire IRBP molecule, and lymphocyte proliferative responses were measured. Peptides determined to be immuno- dominant were used to immunize mice for EAU. Cytokine profile and proliferation of the CD4 versus CD8 subsets were analyzed for the most pathogenic peptides. Results. Two new major pathogenic epitopes were identified in WT C57BL/6 mice, residues 461-480 and 651-670. These epitopes induced EAU of severity similar to that induced by the previously known peptide, 1-20. Several other peptides elicited mild disease with lower incidence. Some peptides elicited EAU only in WT recipients of IRBP KO splenocytes. In the B10.RIII strain, two major new uveito- genic peptides were identified, 171-190 and 541-560, and several others elicited moderate disease. Unlike in C57BL/6 mice, adoptive transfer of WT B10.RIII with IRBP KO spleno- cytes did not reveal additional uveitogenic epitopes. Both CD4 and CD8 lymphocyte subsets proliferated to pathogenic peptides. Conclusions. Several new pathogenic peptides of IRBP were identified in C57BL/6 and B10.RIII mice. Differences in epitope recognition between WT and IRBP KO mice were observed in C57BL/6 mice, but not in B10.RIII mice, suggesting more extensive culling of the repertoire in C57BL/6 mice by endo- genously expressed IRBP.

AB - Purpose. Interphotoreceptor retinoid binding protein (IRBP) is the major uveitogenic retinal antigen eliciting experimental autoimmune uveoretinitis (EAU) in mice. The most frequently used mouse strains are B10.RIII and C57BL/6, but to date only one uveitogenic epitope for each has been identified. The purpose of this study was to identify and characterize additional uveitogenic epitopes in B10.RIII and C57BL/6 mice and to compare epitope recognition in wild-type versus IRBP-defi- cient mice on both backgrounds. Methods. Mice were immunized with IRBP. Spleen cells were stimulated in culture with overlapping peptides representing the entire IRBP molecule, and lymphocyte proliferative responses were measured. Peptides determined to be immuno- dominant were used to immunize mice for EAU. Cytokine profile and proliferation of the CD4 versus CD8 subsets were analyzed for the most pathogenic peptides. Results. Two new major pathogenic epitopes were identified in WT C57BL/6 mice, residues 461-480 and 651-670. These epitopes induced EAU of severity similar to that induced by the previously known peptide, 1-20. Several other peptides elicited mild disease with lower incidence. Some peptides elicited EAU only in WT recipients of IRBP KO splenocytes. In the B10.RIII strain, two major new uveito- genic peptides were identified, 171-190 and 541-560, and several others elicited moderate disease. Unlike in C57BL/6 mice, adoptive transfer of WT B10.RIII with IRBP KO spleno- cytes did not reveal additional uveitogenic epitopes. Both CD4 and CD8 lymphocyte subsets proliferated to pathogenic peptides. Conclusions. Several new pathogenic peptides of IRBP were identified in C57BL/6 and B10.RIII mice. Differences in epitope recognition between WT and IRBP KO mice were observed in C57BL/6 mice, but not in B10.RIII mice, suggesting more extensive culling of the repertoire in C57BL/6 mice by endo- genously expressed IRBP.

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