Psoriasis, T cells and autoimmunity

[1] UM4D4+ (CDW60) T-CELLS ARE COMPARTMENTALIZED INTO PSORIATIC SKIN AND RELEASE LYMPHOKINES THAT INDUCE A KERATINOCYTE PHENOTYPE EXPRESSED IN PSORIATIC LESIONS [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 95 (03) : 275 - 282

[2] BARKER J N W N, 1991, Journal of Dermatological Science, V2, P106, DOI 10.1016/0923-1811(91)90019-T

[3] THE PATHOPHYSIOLOGY OF PSORIASIS [J]. LANCET, 1991, 338 (8761) : 227 - 230

[4] ANTIINFLAMMATORY ACTIONS OF STEROIDS - MOLECULAR MECHANISMS [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 1993, 14 (12) : 436 - 441

[5] FLOW CYTOMETRIC IDENTIFICATION OF PROLIFERATIVE SUBPOPULATIONS WITHIN NORMAL HUMAN EPIDERMIS AND THE LOCALIZATION OF THE PRIMARY HYPERPROLIFERATIVE POPULATION IN PSORIASIS [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (04) : 1271 - 1281

[6] KINETICS AND REGULATION OF HUMAN KERATINOCYTE STEM-CELL GROWTH IN SHORT-TERM PRIMARY EX-VIVO CULTURE - COOPERATIVE GROWTH-FACTORS FROM PSORIATIC LESIONAL T-LYMPHOCYTES STIMULATE PROLIFERATION AMONG PSORIATIC UNINVOLVED, BUT NOT NORMAL, STEM KERATINOCYTES [J]. JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (01) : 317 - 327

[7] CHARACTERIZATION OF MONONUCLEAR CELL INFILTRATES IN PSORIATIC LESIONS [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1978, 71 (05) : 340 - 343

[8] T-CELL-RECEPTOR REPERTOIRE IN CHRONIC PLAQUE-STAGE PSORIASIS IS RESTRICTED AND LACKS ENRICHMENT OF SUPERANTIGEN-ASSOCIATED V-BETA REGIONS [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 104 (05) : 725 - 728

[9] CD8+ T-CELLS IN PSORIATIC LESIONS PREFERENTIALLY USE T-CELL RECEPTOR V(BETA)3 AND/OR V(BETA)13.1 GENES [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (20) : 9282 - 9286

[10] REAPPRAISAL OF IN-SITU IMMUNOPHENOTYPIC ANALYSIS OF PSORIASIS SKIN - INTERACTION OF ACTIVATED HLA-DR(+) IMMUNOCOMPETENT CELLS AND ENDOTHELIAL-CELLS IS A MAJOR FEATURE OF PSORIATIC LESIONS [J]. ARCHIVES OF DERMATOLOGICAL RESEARCH, 1994, 286 (02) : 87 - 96

[1] UM4D4+ (CDW60) T-CELLS ARE COMPARTMENTALIZED INTO PSORIATIC SKIN AND RELEASE LYMPHOKINES THAT INDUCE A KERATINOCYTE PHENOTYPE EXPRESSED IN PSORIATIC LESIONS [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 95 (03) : 275 - 282

[2] BARKER J N W N, 1991, Journal of Dermatological Science, V2, P106, DOI 10.1016/0923-1811(91)90019-T

[3] THE PATHOPHYSIOLOGY OF PSORIASIS [J]. LANCET, 1991, 338 (8761) : 227 - 230

[4] ANTIINFLAMMATORY ACTIONS OF STEROIDS - MOLECULAR MECHANISMS [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 1993, 14 (12) : 436 - 441

[5] FLOW CYTOMETRIC IDENTIFICATION OF PROLIFERATIVE SUBPOPULATIONS WITHIN NORMAL HUMAN EPIDERMIS AND THE LOCALIZATION OF THE PRIMARY HYPERPROLIFERATIVE POPULATION IN PSORIASIS [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (04) : 1271 - 1281

[6] KINETICS AND REGULATION OF HUMAN KERATINOCYTE STEM-CELL GROWTH IN SHORT-TERM PRIMARY EX-VIVO CULTURE - COOPERATIVE GROWTH-FACTORS FROM PSORIATIC LESIONAL T-LYMPHOCYTES STIMULATE PROLIFERATION AMONG PSORIATIC UNINVOLVED, BUT NOT NORMAL, STEM KERATINOCYTES [J]. JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (01) : 317 - 327

[7] CHARACTERIZATION OF MONONUCLEAR CELL INFILTRATES IN PSORIATIC LESIONS [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1978, 71 (05) : 340 - 343

[8] T-CELL-RECEPTOR REPERTOIRE IN CHRONIC PLAQUE-STAGE PSORIASIS IS RESTRICTED AND LACKS ENRICHMENT OF SUPERANTIGEN-ASSOCIATED V-BETA REGIONS [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 104 (05) : 725 - 728

[9] CD8+ T-CELLS IN PSORIATIC LESIONS PREFERENTIALLY USE T-CELL RECEPTOR V(BETA)3 AND/OR V(BETA)13.1 GENES [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (20) : 9282 - 9286

[10] REAPPRAISAL OF IN-SITU IMMUNOPHENOTYPIC ANALYSIS OF PSORIASIS SKIN - INTERACTION OF ACTIVATED HLA-DR(+) IMMUNOCOMPETENT CELLS AND ENDOTHELIAL-CELLS IS A MAJOR FEATURE OF PSORIATIC LESIONS [J]. ARCHIVES OF DERMATOLOGICAL RESEARCH, 1994, 286 (02) : 87 - 96