Literature DB >> 781132

Mechanisms involved in elimination of organisms from experimental cutaneous Candida albicans infections in guinea pigs.

P G Sohnle, M M Frank, C H Kirkpatrick.   

Abstract

Experimental cutaneous Candida albicans infections were produced in guinea pigs either by using occlusive dressings over the organisms or by applying them to the shaved skin directly without occlusive dressings. In either model there was clearance of the infecting organisms from the skin by a process involving profuse scaling of the keratinized layer in which they were confined. However, for each type of infection the mechanisms producing this scaling seemed to involve different parts of the host defense system. Infections produced under occlusive dressings were characterized by a rapid accumulation of polymorphonuclear leukocytes (PMN) in the epidermis and formation of thick crusts in which organisms were trapped. Sloughing of the crust removed the organisms. In this model, evolution of the lesions and the rate of clearance of the organisms did not depend on prior immunity to Candida. Two possible mechanisms for attraction of PMN into the lesions were direct activation of the alternative complement pathway by the organisms in the lesions and direct chemotactic activity in components of Candida albicans. In contrast, infections produced without occlusive dressings showed only minimal epidermal PMN infiltration, but also underwent profuse scaling of the keratinized layer. This response appeared to depend on cell-mediated immunity. Only animals with previously-acquired delayed hypersensitivity to Candida antigens could undergo this type of scaling, and indeed, this response was transferable to nonimmue animals with peritoneal exudate cells from Candida-immune animals. Clearance of the infecting organisms from this type of infection was significantly faster in immune than in nonimmune animals. It is postulated that a lymphokine released from lymphocytes in the upper epidermis acts on epidermal cells to increase the rate of keratin turnover either by the mitotic rate of the germinal cells or by increasing their rate of keratinization.

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Year:  1976        PMID: 781132

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  29 in total

1.  Experimental dermatophytosis in mice: correlation between light and electron microscopic changes in primary, secondary and chronic infections.

Authors:  R J Hay; R A Calderon; C D Mackenzie
Journal:  Br J Exp Pathol       Date:  1988-10

2.  Pathological observations in experimental candida infection of sensitized guinea pigs.

Authors:  M Isoda
Journal:  Mycopathologia       Date:  1985-09       Impact factor: 2.574

3.  Mechanisms of adherence of Candida albicans to cultured human epidermal keratinocytes.

Authors:  M W Ollert; R Söhnchen; H C Korting; U Ollert; S Bräutigam; W Bräutigam
Journal:  Infect Immun       Date:  1993-11       Impact factor: 3.441

4.  Effect of oral tetracycline, the microbial flora, and the athymic state on gastrointestinal colonization and infection of BALB/c mice with Candida albicans.

Authors:  P B Helstrom; E Balish
Journal:  Infect Immun       Date:  1979-03       Impact factor: 3.441

Review 5.  Cutaneous defenses against dermatophytes and yeasts.

Authors:  D K Wagner; P G Sohnle
Journal:  Clin Microbiol Rev       Date:  1995-07       Impact factor: 26.132

6.  Cutaneous basophil hypersensitivity and contact sensitivity after cutaneous Trichophyton mentagrophytes infection.

Authors:  F Green; J W Anderson; E Balish
Journal:  Infect Immun       Date:  1980-08       Impact factor: 3.441

7.  Analysis of transepidermal leukocyte chemotaxis in experimental dermatophytosis in guinea pigs.

Authors:  H Tagami; N Natsume; T Aoshima; F Inoue; S Suehisa; M Yamada
Journal:  Arch Dermatol Res       Date:  1982       Impact factor: 3.017

8.  Immunity to experimental renal candidiasis in rats.

Authors:  T J Rogers; E Balish
Journal:  Infect Immun       Date:  1978-02       Impact factor: 3.441

9.  Inoculation candidiasis in a murine model of severe combined immunodeficiency syndrome.

Authors:  S Mahanty; R A Greenfield; W A Joyce; P W Kincade
Journal:  Infect Immun       Date:  1988-12       Impact factor: 3.441

10.  Experimental murine candidiasis: cell-mediated immunity after cutaneous challenge.

Authors:  S A Moser; J E Domer; F J Mather
Journal:  Infect Immun       Date:  1980-01       Impact factor: 3.441

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