Summary
Experimental cutaneous Candida albicans infections in guinea pigs are histologically characterized by intense epidermal polymorphonuclear leukocyte (PMN) accumulation. To study the role of PMNs in vivo, we injected 250 μcolchicine/kg i.p., a strong inhibitor of PMN chemotaxis, and observed the influence of reduced PMN migration in experimental cutaneous candidiasis with special interest in the elimination course of the organisms.
There was a significant delay in the clearance of the organisms in the colchicine-treated group with decreased epidermal PMN infiltration and prolonged visible scaling process.
Our data suggest that the delay of epidermal PMN migration parallels the disappearance of the organisms from the infected skin and that PMNs play an important part in defense against candida infections especially in the elimination process.
Zusammenfassung
Experimentelle Hautinfektion mit Candida albicans bei Meerschweinchen wird histologisch durch intensive epidermische Akkumulation der polymorphonuclearen Leukocyten (PMN) charakterisiert. Um die Rollen der PMN in vivo zu studieren, injizierten wir i.p. 250 μg Colchicin/kg, einen potenten Inhibitor der PMN-Chemotaxis, und beobachteten Einflüsse der reduzierten PMN-Migration bei der experimentellen Candidiasis, mit spezialem Interesse am Eliminationsverlauf des Organismus.
Es gab bei der Colchicin-behandelten Gruppe eine signifikante Verzögerung mit der Abnahme der epidermischen PMN-Infiltration und der Verlängerung des sichtbaren Schuppenprozesses.
Unsere Daten zeigen, daß die Verzögerung der epidermischen PMN-Migration dem Verschwinden des Organismus aus der infizierten Haut entspricht und daß PMN in der Abwehr gegen die Candida-Infektion, besonders in dem Eliminationsverlauf, eine wichtige Rolle spielen.
Similar content being viewed by others
References
Belcher RW, Carney JF, Monahan FG (1973) An electron-microscopic study of phagocytosis of Candida albicans by polymorphonuclear leukocytes. Lab Invest 29:620–627
Bodey GP (1966) Fungal infections complicating acute leukemia. J Chronic Dis 19:667–687
Van Custem J, Thienpont D (1971) Experimental cutaneous Candida albicans infection in guinea pigs. Sabouraudia 9:17–20
Denning TJV, Davies RR (1973) Candida albicans and the chemotaxis of polymorphonuclear neutrophils. Sabouraudia 11:210–221
Kim Oh MH, Rodey GE, Good RA, Chilgren RA, Quie PG (1969) Defective candidacidal capacity of polymorphonuclear leukocytes in chronic granulomatous disease of childhood. J Pediatr 75:300–303
Lehrer RI, Cline MJ (1969) Interaction of Candida albicans with human leukocytes and serum. J Bacteriol 98:996–1004
Louria DB, Brayton RG, Finkel G (1963) Studies of the pathogenesis of experimental Candida albicans infections in mice. Sabouraudia 2:271–283
Miyachi Y, Takigawa M, Imamura S (1981) Suppressions of DNCB-induced irritant dermatitis by colchicine. Acta Derm Venereol (Stockh) 61:307–311
Morelli R, Rosenberg LT (1971) Role of complement during experimental Candida infection in mice. Infect Immun 3:521–523
Morelli R, Rosenberg LT (1971) The role of complement in the phagocytosis of Candida albicans by mouse peripheral blood leukocytes. J Immunol 107:476–480
Ray TL, Wuepper KD (1976) Experimental cutaneous candidiasis in rodents. J Invest Dermatol 66:29–33
Ray TL, Wuepper KD (1976) Activation of the alternative (properdin) pathway of complement by Candida albicans and related species. J Invest Dermatol 67:700–703
Ray TL, Wuepper KD (1978) Experimental candidiasis in rodents. II. Role of the stratum corneum barrier and serum complement as a mediator of a protective inflammatory response. Arch Dermatol 114:539–543
Ray TL, Hanson A, Ray LF, Wuepper KD (1979) Purification of a mannan from Candida albicans which activates serum complement. J Invest Dermatol 73:269–274
Rebora A, Marples RR, Kligman AM (1973) Experimental infection with Candida albicans. Arch Dermatol 108:69–73
Scherwitz C, Martin R (1979) The phagocytosis of Candida albicans blastospores and germ tubes by polymorphonuclear leukocytes. Dermatologica 159:12–23
Van Scoy RE, Hill HR, Ritts RE, Quie PG (1975) Familial neutrophil chemotaxis defect, recurrent bacterial infections, mucocutaneous candidiasis, and hyperimmunoglobulinemia E. Ann Intern Med 82:766–771
Sohnle PG, Frank MM, Kirkpatrick CH (1976) Mechanisms involved in elimenation of organisms from experimental cutaneous Candida albicans infections in guinea pigs. J Immunol 117:523–530
Sohnle PG, Frank MM, Kirkpatrick CH (1976) Deposition of complement components in the cutaneous lesions of chronic mucocutaneous candidiasis. Clin Immunol Immunopathol 5:340–350
Tagami H, Watanabe S, Ofuji S (1973) Trichophytin contact sensitivity in guinea pigs with experimental dermatophytosis induced by a new inoculation method. J Invest Dermatol 61:237–241
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Miyachi, Y., Horio, T. & Imamura, S. The fate of experimental cutaneous candidiasis in guinea pigs under the suppressed polymorphonuclear leukocyte chemotaxis by colchicine. Arch Dermatol Res 271, 373–380 (1981). https://doi.org/10.1007/BF00406681
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00406681