
Tissa Hata, M.D.
· HS Clinical Professor of DermatologyVerifiedUniversity of California, San Diego · Dermatology
Active 1954–2025
About
Tissa Hata, M.D., is a Clinical Professor of Dermatology at UC San Diego School of Medicine. His research focuses on the role of the skin microbiome, skin barrier function, and the pathophysiology of dermatologic diseases such as atopic dermatitis, rosacea, and acne. He has contributed to establishing the significance of Staphylococcus aureus in dermatologic conditions and exploring microbiome-targeted treatments, including bacteriotherapy and topical therapies. Dr. Hata's work involves investigating the genetic, molecular, and cellular mechanisms underlying skin inflammation and infection, with a particular interest in how skin microbiota influence disease severity and treatment outcomes.
Research topics
- Immunology
- Microbiology
- Biology
- Medicine
- Internal medicine
- Cell biology
- Biochemistry
- Dermatology
Selected publications
Journal of Investigative Dermatology · 2025-11-01
article0428 Correlates to barrier function before and after dupilumab treatment
Journal of Investigative Dermatology · 2025-07-21
articleOpen accessMicrobiome as a Potential Target for Treatment and Prevention of Atopic Dermatitis
Immunology and Allergy Clinics of North America · 2025-08-23 · 1 citations
reviewSenior authorCorrespondingJournal of Investigative Dermatology · 2025-07-21
articleSenior authorJournal of Investigative Dermatology · 2025-09-24 · 1 citations
articleOpen accessSenior authorJournal of Allergy and Clinical Immunology · 2024-02-01 · 1 citations
articleOpen accessTopical Ivermectin Treatment of Rosacea Changes the Bacterial Microbiome of the Skin
Journal of Investigative Dermatology · 2024-10-30 · 5 citations
articleOpen accessSenior authorCXCL12+ dermal fibroblasts promote neutrophil recruitment and host defense by recognition of IL-17
The Journal of Experimental Medicine · 2024-02-23 · 46 citations
articleOpen accessThe skin provides an essential barrier for host defense through rapid action of multiple resident and recruited cell types, but the complex communication network governing these processes is incompletely understood. To define these cell-cell interactions more clearly, we performed an unbiased network analysis of mouse skin during invasive S. aureus infection and revealed a dominant role for CXCL12+ fibroblast subsets in neutrophil communication. These subsets predominantly reside in the reticular dermis, express adipocyte lineage markers, detect IL-17 and TNFα, and promote robust neutrophil recruitment through NFKBIZ-dependent release of CXCR2 ligands and CXCL12. Targeted deletion of Il17ra in mouse fibroblasts resulted in greatly reduced neutrophil recruitment and increased infection by S. aureus. Analogous human CXCL12+ fibroblast subsets abundantly express neutrophil chemotactic factors in psoriatic skin that are subsequently decreased upon therapeutic targeting of IL-17. These findings show that CXCL12+ dermal immune acting fibroblast subsets play a critical role in cutaneous neutrophil recruitment and host defense.
Journal of Investigative Dermatology · 2024-07-19
articleOpen accessSenior authorCERS1 is a biomarker of Staphylococcus aureus abundance and atopic dermatitis severity
Journal of Allergy and Clinical Immunology · 2024-09-27 · 8 citations
articleOpen access
Frequent coauthors
- 166 shared
Richard L. Gallo
University of California, San Diego
- 110 shared
Lisa A. Beck
Mayo Clinic in Arizona
- 90 shared
Robert A. Swerlick
Emory University
- 83 shared
Nicole L. Ward
Vanderbilt University
- 81 shared
Ethan A. Lerner
- 81 shared
Stephen I. Katz
Trent University
- 81 shared
Kim B. Yancey
The University of Texas Southwestern Medical Center
- 81 shared
Janet A. Fairley
Education
M.D.
University of California, San Diego
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