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Chemokine Signaling in Allergic Contact Dermatitis: Toward Targeted Therapies

Journal

DERMATITIS
Volume 29, Issue 4, Pages 179-186

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/DER.0000000000000391

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Funding

  1. Burroughs Wellcome Career Award for Medical Scientists
  2. Duke Pinnell Center for Investigative Dermatology
  3. [T32GM7171]
  4. [1R01GM122798-01A1]
  5. [K08HL114643-01A1]

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Allergic contact dermatitis (ACD) is a common skin disease that results in significant cost and morbidity. Despite its high prevalence, therapeutic options are limited. Allergic contact dermatitis is regulated primarily by T cells within the adaptive immune system, but also by natural killer and innate lymphoid cells within the innate immune system. The chemokine receptor system, consisting of chemokine peptides and chemokine G protein-coupled receptors, is a critical regulator of inflammatory processes such as ACD. Specific chemokine signaling pathways are selectively up-regulated in ACD, most prominently CXCR3 and its endogenous chemokines CXCL9, CXCL10, and CXCL11. Recent research demonstrates that these 3 chemokines are not redundant and indeed activate distinct intracellular signaling profiles such as those activated by heterotrimeric G proteins and -arrestin adapter proteins. Such differential signaling provides an attractive therapeutic target for novel therapies for ACD and other inflammatory diseases.

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