|
|
||||||||
1 From the Laboratory of Immunology, 3 Laboratory of Molecular and Developmental Biology, National Eye Institute, National Institutes of Health, Bethesda, Maryland; and the 2 Howard Hughes Medical InstituteNational Institutes of Health Research Scholars Program, Bethesda, Maryland.
PURPOSE. Sight-damaging ocular inflammation is often mediated by T-helper (Th) lymphocytes. The population of Th cells is divided into two major subsets, designated Th1 and Th2, that differ by their cytokine production and biological activities. In the present study, the capacity of Th1 and Th2 cells to induce ocular inflammation was examined.
METHODS. Ocular inflammation was induced in transgenic (Tg) mice that express hen egg lysozyme (HEL) in their lens, by adoptively transferring Th cells that transgenically express HEL-specific receptor. Th1 and Th2 populations were polarized in vitro, and their selective cytokine production was determined by conventional methods. Levels of ocular inflammation were monitored by conventional histologic methods. Infiltrating cells were collected from sections of inflamed eyes by microdissection, and their cytokine production was examined by RT-PCR.
RESULTS. Th1 cells were highly immunopathogenic, producing disease in naive recipients at numbers as low as 0.12 x 106, whereas Th2 cells were inactive in these recipients, even at 30 x 106. Th2 cells, however, produced inflammation when transferred into sublethally irradiated recipients. Distinctive histopathologic changes characterized ocular inflammation induced by the two types of Th cells. Cytokine analysis of infiltrating cells in recipient mouse eyes, as well as of splenocytes of these mice demonstrated that the transferred cells retained their type specificity. Coinjecting Th2 and Th1 cells did not alleviate the ocular disease in naive recipients and even exacerbated the immunopathogenic process in irradiated recipients.
CONCLUSIONS. Th2 cells are capable of inducing ocular inflammation, but only in immunodeficient mice, and are profoundly inferior to Th1 cells in their immunopathogenic capacity.
This article has been cited by other articles:
![]() |
C. A. Cox, G. Shi, H. Yin, B. P. Vistica, E. F. Wawrousek, C.-C. Chan, and I. Gery Both Th1 and Th17 Are Immunopathogenic but Differ in Other Key Biological Activities J. Immunol., June 1, 2008; 180(11): 7414 - 7422. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. G.-J. Ooi, G. Galatowicz, V. L. Calder, and S. L. Lightman Cytokines and Chemokines in Uveitis - Is there a Correlation with Clinical Phenotype? Clin. Med. Res., December 1, 2006; 4(4): 294 - 309. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Fujimoto, C.-R. Yu, G. Shi, B. P. Vistica, E. F. Wawrousek, D. M. Klinman, C.-C. Chan, C. E. Egwuagu, and I. Gery Pertussis Toxin Is Superior to TLR Ligands in Enhancing Pathogenic Autoimmunity, Targeted at a Neo-Self Antigen, by Triggering Robust Expansion of Th1 Cells and Their Cytokine Production J. Immunol., November 15, 2006; 177(10): 6896 - 6903. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Chen, C. Fujimoto, B. P. Vistica, E. F. Wawrousek, B. Kelsall, and I. Gery Active participation of antigen-nonspecific lymphoid cells in immune-mediated inflammation. J. Immunol., September 1, 2006; 177(5): 3362 - 3368. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. Toscano, A. G. Commodaro, J. M. Ilarregui, G. A. Bianco, A. Liberman, H. M. Serra, J. Hirabayashi, L. V. Rizzo, and G. A. Rabinovich Galectin-1 Suppresses Autoimmune Retinal Disease by Promoting Concomitant Th2- and T Regulatory-Mediated Anti-Inflammatory Responses J. Immunol., May 15, 2006; 176(10): 6323 - 6332. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. J. Curnow, F. Falciani, O. M. Durrani, C. M. G. Cheung, E. J. Ross, K. Wloka, S. Rauz, G. R. Wallace, M. Salmon, and P. I. Murray Multiplex Bead Immunoassay Analysis of Aqueous Humor Reveals Distinct Cytokine Profiles In Uveitis Invest. Ophthalmol. Vis. Sci., November 1, 2005; 46(11): 4251 - 4259. [Abstract] [Full Text] [PDF] |
||||
![]() |
W.-K. Lim, C. Fujimoto, R. Ursea, S. P. Mahesh, P. Silver, C.-C. Chan, I. Gery, and R. B. Nussenblatt Suppression of Immune-Mediated Ocular Inflammation in Mice by Interleukin 1 Receptor Antagonist Administration Arch Ophthalmol, July 1, 2005; 123(7): 957 - 963. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-R. Yu, R. M. Mahdi, S. Ebong, B. P. Vistica, J. Chen, Y. Guo, I. Gery, and C. E. Egwuagu Cell Proliferation and STAT6 Pathways Are Negatively Regulated in T Cells by STAT1 and Suppressors of Cytokine Signaling J. Immunol., July 15, 2004; 173(2): 737 - 746. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Bo Su, P. B. Silver, P. Wang, C.-C. Chan, and R. R. Caspi Cholera Toxin Prevents Th1-Mediated Autoimmune Disease by Inducing Immune Deviation J. Immunol., July 15, 2004; 173(2): 755 - 761. [Abstract] [Full Text] [PDF] |
||||
![]() |
D.-I. Ham, S. J. Kim, J. Chen, B. P. Vistica, R. N. Fariss, R. S. Lee, E. F. Wawrousek, H. Takase, C.-R. Yu, C. E. Egwuagu, et al. Central Immunotolerance in Transgenic Mice Expressing a Foreign Antigen under Control of the Rhodopsin Promoter Invest. Ophthalmol. Vis. Sci., March 1, 2004; 45(3): 857 - 862. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Xu, A. Manivannan, H.-R. Jiang, J. Liversidge, P. F. Sharp, J. V. Forrester, and I. J. Crane Recruitment of IFN-{gamma}-Producing (Th1-Like) Cells into the Inflamed Retina In Vivo Is Preferentially Regulated by P-Selectin Glycoprotein Ligand 1:P/E-Selectin Interactions J. Immunol., March 1, 2004; 172(5): 3215 - 3224. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-R. Yu, R. M. Mahdi, S. Ebong, B. P. Vistica, I. Gery, and C. E. Egwuagu Suppressor of Cytokine Signaling 3 Regulates Proliferation and Activation of T-helper Cells J. Biol. Chem., August 8, 2003; 278(32): 29752 - 29759. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |