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DOI 10.1111/j.1440-0960.2010.00717.x

Медицинская библиотека · The Australasian journal of dermatology · 2011

Enfuvirtide injection site reactions: a clinical and histopathological appraisal.

Wallace Brian J, Tan King-Bing, Pett Sarah L, Cooper David A, Kossard Steven, Whitfeld Margot J

Клинический случайСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND/

OBJECTIVES

Enfuvirtide was the first of a new class of antiretroviral agents termed 'fusion inhibitors' used for the treatment of HIV-1 infection. Enfuvirtide is administered subcutaneously and injection site reactions (ISR) are commonplace (98%). The aim of this study was to analyse in detail the histopathological changes associated with striking ISR seen in four patients.

METHODS

Biopsies were obtained at various times post-injection and were reviewed histologically. The changes in epidermal, dermal and subcutaneous connective tissue and the presence and nature of the inflammatory cellular infiltrate were noted. An immunohistochemical assessment was undertaken.

RESULTS

All biopsy specimens demonstrated striking changes in the dermal connective tissue. Alteration in collagen was the most prominent feature and resembled a morphoea/scleroderma-like process. These changes persisted well beyond cessation of enfuvirtide (>1 year). The relative populations of dermal dendritic cells (DDC) (types 1 (Factor XIIIa) and 2 (CD34+)) were analysed and a reciprocal relationship between DDC subpopulations was observed akin to that observed in other sclerosing and fibrosing conditions.

CONCLUSION

This study details histopathological changes associated with enfuvirtide ISR. We postulate that changes in DDC populations may contribute to the pathogenesis of the sclerotic process observed with enfuvirtide ISR.

Для цитирования: Wallace Brian J, Tan King-Bing, Pett Sarah L, Cooper David A, Kossard Steven, Whitfeld Margot J. Enfuvirtide injection site reactions: a clinical and histopathological appraisal.. The Australasian journal of dermatology. 2011. DOI: 10.1111/j.1440-0960.2010.00717.x.

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