Abstract
Alopecia areata is a tissue-restricted autoimmune disease of the hair follicle, which results in hair loss and baldness. It is often psychologically devastating. The role of T lymphocytes in this disorder was investigated with cell transfer experiments. Scalp explants from patients were transplanted to severe combined immunodeficiency (SCID) mice and injected with autologous T lymphocytes isolated from involved scalp. T lymphocytes which had been cultured with hair follicle homogenate along with antigen-presenting cells were capable of inducing the changes of alopecia areata, including hair loss and perifollicular infiltrates of T cells, along with HLA-DR and ICAM-1 expression of the follicular epithelium. Similar changes were not noted in grafts injected with scalp-derived T cells that had not been cultured with follicular homogenate. These data indicate that alopecia areata is mediated by T cells which recognize a follicular autoantigen.
Full Text
The Full Text of this article is available as a PDF (469.1 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Boehncke W. H., Dressel D., Zollner T. M., Kaufmann R. Pulling the trigger on psoriasis. Nature. 1996 Feb 29;379(6568):777–777. doi: 10.1038/379777a0. [DOI] [PubMed] [Google Scholar]
- Colón E. A., Popkin M. K., Callies A. L., Dessert N. J., Hordinsky M. K. Lifetime prevalence of psychiatric disorders in patients with alopecia areata. Compr Psychiatry. 1991 May-Jun;32(3):245–251. doi: 10.1016/0010-440x(91)90045-e. [DOI] [PubMed] [Google Scholar]
- Duvic M., Hordinsky M. K., Fiedler V. C., O'Brien W. R., Young R., Reveille J. D. HLA-D locus associations in alopecia areata. DRw52a may confer disease resistance. Arch Dermatol. 1991 Jan;127(1):64–68. [PubMed] [Google Scholar]
- Gilhar A., Krueger G. G. Hair growth in scalp grafts from patients with alopecia areata and alopecia universalis grafted onto nude mice. Arch Dermatol. 1987 Jan;123(1):44–50. [PubMed] [Google Scholar]
- Gilhar A., Pillar T., Assay B., David M. Failure of passive transfer of serum from patients with alopecia areata and alopecia universalis to inhibit hair growth in transplants of human scalp skin grafted on to nude mice. Br J Dermatol. 1992 Feb;126(2):166–171. doi: 10.1111/j.1365-2133.1992.tb07815.x. [DOI] [PubMed] [Google Scholar]
- Gilhar A., Pillar T., David M., Eidelman S. Melanocytes and Langerhans cells in aged versus young skin before and after transplantation onto nude mice. J Invest Dermatol. 1991 Feb;96(2):210–214. doi: 10.1111/1523-1747.ep12461330. [DOI] [PubMed] [Google Scholar]
- Gilhar A., Pillar T., Etzioni A. The effect of topical cyclosporin on the immediate shedding of human scalp hair grafted onto nude mice. Br J Dermatol. 1988 Dec;119(6):767–770. doi: 10.1111/j.1365-2133.1988.tb03501.x. [DOI] [PubMed] [Google Scholar]
- Kalish R. S., Johnson K. L. Enrichment and function of urushiol (poison ivy)-specific T lymphocytes in lesions of allergic contact dermatitis to urushiol. J Immunol. 1990 Dec 1;145(11):3706–3713. [PubMed] [Google Scholar]
- Kalish R. S., Johnson K. L., Hordinsky M. K. Alopecia areata. Autoreactive T cells are variably enriched in scalp lesions relative to peripheral blood. Arch Dermatol. 1992 Aug;128(8):1072–1077. doi: 10.1001/archderm.128.8.1072. [DOI] [PubMed] [Google Scholar]
- Khoury E. L., Price V. H., Greenspan J. S. HLA-DR expression by hair follicle keratinocytes in alopecia areata: evidence that it is secondary to the lymphoid infiltration. J Invest Dermatol. 1988 Feb;90(2):193–200. doi: 10.1111/1523-1747.ep12462213. [DOI] [PubMed] [Google Scholar]
- McElwee K. J., Spiers E. M., Oliver R. F. In vivo depletion of CD8+ T cells restores hair growth in the DEBR model for alopecia areata. Br J Dermatol. 1996 Aug;135(2):211–217. [PubMed] [Google Scholar]
- Messenger A. G., Bleehen S. S. Expression of HLA-DR by anagen hair follicles in alopecia areata. J Invest Dermatol. 1985 Dec;85(6):569–572. doi: 10.1111/1523-1747.ep12277414. [DOI] [PubMed] [Google Scholar]
- Milgraum S. S., Mitchell A. J., Bacon G. E., Rasmussen J. E. Alopecia areata, endocrine function, and autoantibodies in patients 16 years of age or younger. J Am Acad Dermatol. 1987 Jul;17(1):57–61. doi: 10.1016/s0190-9622(87)70170-4. [DOI] [PubMed] [Google Scholar]
- Nickoloff B. J., Griffiths C. E. Aberrant intercellular adhesion molecule-1 (ICAM-1) expression by hair-follicle epithelial cells and endothelial leukocyte adhesion molecule-1 (ELAM-1) by vascular cells are important adhesion-molecule alterations in alopecia areata. J Invest Dermatol. 1991 May;96(5):91S–92S. doi: 10.1111/1523-1747.ep12472216. [DOI] [PubMed] [Google Scholar]
- Paus R., Slominski A., Czarnetzki B. M. Is alopecia areata an autoimmune-response against melanogenesis-related proteins, exposed by abnormal MHC class I expression in the anagen hair bulb? Yale J Biol Med. 1993 Nov-Dec;66(6):541–554. [PMC free article] [PubMed] [Google Scholar]
- Perret C., Wiesner-Menzel L., Happle R. Immunohistochemical analysis of T-cell subsets in the peribulbar and intrabulbar infiltrates of alopecia areata. Acta Derm Venereol. 1984;64(1):26–30. [PubMed] [Google Scholar]
- Tobin D. J., Hann S. K., Song M. S., Bystryn J. C. Hair follicle structures targeted by antibodies in patients with alopecia areata. Arch Dermatol. 1997 Jan;133(1):57–61. [PubMed] [Google Scholar]
- Todes-Taylor N., Turner R., Wood G. S., Stratte P. T., Morhenn V. B. T cell subpopulations in alopecia areata. J Am Acad Dermatol. 1984 Aug;11(2 Pt 1):216–223. doi: 10.1016/s0190-9622(84)70152-6. [DOI] [PubMed] [Google Scholar]
- Wrone-Smith T., Nickoloff B. J. Dermal injection of immunocytes induces psoriasis. J Clin Invest. 1996 Oct 15;98(8):1878–1887. doi: 10.1172/JCI118989. [DOI] [PMC free article] [PubMed] [Google Scholar]