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Melanocyte-associated T cell epitopes can function as autoantigens for transfer of alopecia areata to human scalp explants on Prkdc(scid) mice.

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The Journal of investigative dermatology 📖 저널 OA 67.9% 2021: 20/22 OA 2022: 11/14 OA 2023: 14/29 OA 2024: 15/36 OA 2025: 36/70 OA 2026: 32/69 OA 2021~2026 2001 Vol.117(6) p. 1357-62 피인용 23회 cited 152 RCR 2.78
TL;DR Melanocyte-peptide-activated T cells significantly reduced the number of hairs regrowing in two experiments with six patients, suggesting epitope spreading in alopecia areata.
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PubMed DOI Semantic 마지막 보강 2026-05-10
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Gilhar A, Landau M, Assy B, Shalaginov R, Serafimovich S, Kalish RS

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Melanocyte-peptide-activated T cells significantly reduced the number of hairs regrowing in two experiments with six patients, suggesting epitope spreading in alopecia areata.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • p-value p <0.01
  • p-value p <0.001

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↓ .bib ↓ .ris
APA Gilhar A, Landau M, et al. (2001). Melanocyte-associated T cell epitopes can function as autoantigens for transfer of alopecia areata to human scalp explants on Prkdc(scid) mice.. The Journal of investigative dermatology, 117(6), 1357-62. https://doi.org/10.1046/j.0022-202x.2001.01583.x
MLA Gilhar A, et al.. "Melanocyte-associated T cell epitopes can function as autoantigens for transfer of alopecia areata to human scalp explants on Prkdc(scid) mice.." The Journal of investigative dermatology, vol. 117, no. 6, 2001, pp. 1357-62.
PMID 11886495 ↗

Abstract

Alopecia areata is a tissue restricted autoimmune condition affecting the hair follicle, resulting in hair loss. The goal of this study was to test the hypothesis that the autoantigen of alopecia areata is melanocyte associated. Potential autoantigens were tested in the human scalp explant/Prkd(scid) CB-17 mouse transfer system. Scalp T cells from lesional (bald) alopecia areata scalp were cultured with antigen-presenting cells, and antigen, along with interleukin-2. The T cells were then injected into autologous lesional scalp grafts on SCID mice, and hair regrowth was measured. Hair follicle homogenate was used as an autoantigen control. T cells cultured with melanoma homogenate induced statistically significant reduction in hair growth (p <0.01 by ANOVA). HLA-A2-restricted melanocyte peptide epitopes were then tested with lesional scalp T cells from HLA-A2-positive alopecia areata patients. Melanocyte-peptide-activated T cells significantly reduced the number of hairs regrowing in two experiments with six patients (p <0.001 by ANOVA). Injected scalp grafts showed histologic and immunochemical changes of alopecia areata. The most consistent peptide autoantigens were the Gp100-derived G9-209 and G9-280 peptides, as well as MART-1 (27-35). Melanocyte peptide epitopes can function as autoantigens for alopecia areata. Multiple peptides were recognized, suggesting epitope spreading.

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그래프 OA 노드: 7/8 (88%) · 참조 0편 · 후속 7편

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