Circulating CD8+T cells in polymyalgia rheumatica and giant cell arteritis: A review

Citation
Vm. Martinez-taboada et al., Circulating CD8+T cells in polymyalgia rheumatica and giant cell arteritis: A review, SEM ARTH RH, 30(4), 2001, pp. 257-271
Citations number
97
Categorie Soggetti
Rheumatology
Journal title
SEMINARS IN ARTHRITIS AND RHEUMATISM
ISSN journal
00490172 → ACNP
Volume
30
Issue
4
Year of publication
2001
Pages
257 - 271
Database
ISI
SICI code
0049-0172(200102)30:4<257:CCCIPR>2.0.ZU;2-1
Abstract
Background and Objective: During the last few years, there have been severa l studies on T cell subsets in polymyalgia rheumatica (PMR) and giant cell arteritis (GCA), with conflicting results. Whereas some authors have found normal values of circulating CD8+ T cells, others have found a decreased nu mber. Furthermore, in some studies, the level of CD8+ cells was found to be related to disease activity, and it has been proposed that a decrease of C D8+ T cells be used as a diagnostic criterion for PMR. The purpose of our s tudy was to determine the value of assessing T cell subsets in PMR and GCA. Methods: T lymphocyte subsets were determined by flow cytometry using a who le blood lysis technique in the following groups: 28 PMR and 6 GCA patients before corticosteroid treatment, 20 PMR and 12 GCA patients in clinical re mission with steroid treatment, 55 PMR patients in remission without steroi d treatment, 17 rheumatoid arthritis (RA) patients before treatment, and 18 age-matched controls with noninflammatory conditions. Total white cell, ly mphocyte, and platelet counts, hemoglobin, C-reactive protein (CRP), and er ythrocyte sedimentation rate (ESR) were measured by routine techniques. Com parisons were made by the Student's t-test and the Mann-Whitney test. A MED LINE database search far studies published between 1983 and 1997 was perfor med. Results: Compared with noninflammatory controls, CD8+ T cells were not redu ced before steroid treatment in patients with active PMR/GCA in proportion (P =.7) or absolute numbers (P =.1). patients with active disease had signi ficantly lower hemoglobin levels and higher platelet counts, CRP, and ESR t han noninflammatory controls (P <.05). When compared with active RA, CD8+ T cells were not reduced in patients with active PMR in proportion (P =.5) o r absolute numbers (P =.2). Between these two groups, RA patients were sign ificantly younger (P =.003) and had lower ESR values (P =.003). We did not find significant differences between patients with active PMR/GCA and those in remission with steroid therapy, except for the lower hemoglobin levels and higher platelet count, CRP, and ESR in the active disease group (P <.05 ). The same results were found when patients with active disease were compa red with PMR in remission and no longer on steroid therapy, the only signif icant differences were those parameters reflecting the acute phase response (hemoglobin levels, platelet count, CRP and ESR). Conclusions: This study does not confirm the previous findings that the pro portion or number of circulating CD8+ T cells are reduced in patients with active PMR/GCA. The utility of the determination of CD8+ T cells for diagno stic and prognostic purpose should be evaluated in a large multicenter stud y, Semin Arthritis Rheum 30:257-271. Copyright (C) 2001 by W.B. Saunders Co mpany.