Psoriatic arthritis joint fluids are characterized by CD8 and CD4 T cell clonal expansions that appear antigen driven

被引:91
作者
Costello, PJ
Winchester, RJ
Curran, SA
Peterson, KS
Kane, DJ
Bresnihan, B
FitzGerald, OM
机构
[1] St Vincents Univ Hosp, Dept Rheumatol, Educ & Res Ctr, Dublin 4, Ireland
[2] Columbia Univ Coll Phys & Surg, New York, NY 10032 USA
关键词
D O I
10.4049/jimmunol.166.4.2878
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The CD8 alpha betaT cell receptor repertoire In joint fluid of individuals with active psoriatic arthritis contained an average of 32 major oligoclonal expansions in many variable genes of the TCR beta chain (BV) families, as shown by beta chain CDR3 length analysis. Interestingly; a small number of oligoclonal expansions mere shared between simultaneous samples of joint fluid and blood; however, most expansions found in joint fluid were not identifiable in blood emphasizing the immunologic specificity of the clonal events for the inflamed joint at a given point of time. The CD4 T cell joint fluid repertoire contained fewer and smaller oligoclonal expansions also largely restricted to the joint, suggesting that CD4T cells participate perhaps by interacting cognitively to generate the CD8 clones. The inferred amino acid sequence of a single CD8 oligoclonal expansion revealed that they usually are composed of one or a few structurally related clones at the amino acid sequence level with beta -chains that encode identical or highly homologous CDR3 motifs, These were not shared among patients. Moreover, several clones that encoded the same amino acid sequence were found to be structurally distinct at the nucleotide level, strongly implying clonal selection and expansion is operating at the level of specific TCR-peptide interactions. The findings support a model of psoriatic arthritis inflammation involving extensive and selective Ag, likely autoantigen, driven intra-articular CD4, and CD8 T cell clonal expansions.
引用
收藏
页码:2878 / 2886
页数:9
相关论文
共 55 条
[1]  
Arden Bernhard, 1995, Immunogenetics, V42, P455
[2]  
ARNETT FC, 1980, ARTHRITIS RHEUM, V23, P649
[3]   HUMAN T-CELL RECEPTOR GENE NOMENCLATURE [J].
CONCANNON, P ;
ROBINSON, MA .
T-CELL RECEPTOR USE IN HUMAN AUTOIMMUNE DISEASES, 1995, 756 :124-129
[4]  
Costello P, 1999, J RHEUMATOL, V26, P1117
[5]  
Costello P, 1997, ARTHRITIS RHEUM, V40, P36
[6]   THE PRESUMPTIVE CDR3 REGIONS OF BOTH T-CELL RECEPTOR ALPHA-CHAIN AND BETA-CHAIN DETERMINE T-CELL SPECIFICITY FOR MYOGLOBIN PEPTIDES [J].
DANSKA, JS ;
LIVINGSTONE, AM ;
PARAGAS, V ;
ISHIHARA, T ;
FATHMAN, CG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (01) :27-33
[7]   TCRB clonotypes are present in CD4+ T cell populations prepared directly from rheumatoid synovium [J].
Davey, MP ;
Burgoine, GA ;
Woody, CN .
HUMAN IMMUNOLOGY, 1997, 55 (01) :11-21
[8]  
Dulphy N, 1999, J IMMUNOL, V162, P3830
[9]   ACQUIRED-IMMUNODEFICIENCY-SYNDROME - ASSOCIATED PSORIASIS AND REITERS-SYNDROME [J].
DUVIC, M ;
JOHNSON, TM ;
RAPINI, RP ;
FREESE, T ;
BREWTON, G ;
RIOS, A .
ARCHIVES OF DERMATOLOGY, 1987, 123 (12) :1622-1632
[10]   CHARACTERIZATION OF THE PRIMARY STRUCTURE OF T-CELL RECEPTOR-BETA CHAINS IN CELLS INFILTRATING THE SALIVARY-GLAND IN THE SICCA SYNDROME OF HIV-1 INFECTION - EVIDENCE OF ANTIGEN-DRIVEN CLONAL SELECTION SUGGESTED BY RESTRICTED COMBINATIONS OF V-BETA J-BETA GENE SEGMENT USAGE AND SHARED SOMATICALLY ENCODED AMINO-ACID-RESIDUES [J].
DWYER, E ;
ITESCU, S ;
WINCHESTER, R .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (01) :495-502