Leishmanial antigens in the diagnosis of active lesions and ancient scars of American tegumentary leishmaniasis patients

被引:47
|
作者
Schubach, A
Cuzzi-Maya, T
Oliveira, AV
Sartori, A
de Oliveira-Neto, MP
Mattos, MS
Araújo, ML
Souza, WJS
Haddad, F
Perez, MD
Pacheco, RS
Momen, H
Coutinho, SG
Marzochi, MCD
Marzochi, KBF
da Costa, SCG
机构
[1] Fiocruz MS, Ctr Pesquisa Hosp Evandro Chagas, BR-21045900 Rio De Janeiro, RJ, Brazil
[2] Univ Estadual Paulista Julio Mesquita Filho, Dept Microbiol & Immunol, Botucatu, SP, Brazil
[3] Fiocruz MS, Dept Bioquim & Biol Mol, BR-21045900 Rio De Janeiro, RJ, Brazil
[4] Fiocruz MS, Inst Oswaldo Cruz, Dept Protozool, BR-21045900 Rio De Janeiro, RJ, Brazil
[5] Univ Estado Rio De Janeiro, Dept Patol, Rio De Janeiro, RJ, Brazil
[6] Hosp Geral De Bonsucesso, Serv Endoscopia Peroral, Rio De Janeiro, RJ, Brazil
来源
MEMORIAS DO INSTITUTO OSWALDO CRUZ | 2001年 / 96卷 / 07期
关键词
American tegumentary leishmaniasis; Leishmania (Viannia) braziliensis; immunodiagnosis; scar; cured patients;
D O I
10.1590/S0074-02762001000700018
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Cutaneous biopsies (n = 94) obtained from 88 patients with American tegumentary leishmaniasis were studied by conventional and immunohistochemical techniques. Specimens were distributed as active lesions of cutaneous leishmaniasis (n = 53) (Group I), cicatricial lesions of cutaneous leishmaniasis (n = 35) (Group II) and suggestive scars of healed mucosal leishmaniasis patients (n = 6) (Group III). In addition, active cutaneous lesions of other etiology (n = 24) (Group C1) and cutaneous scars not related to leishmaniasis (n = 10) (Group C2) were also included in the protocol. Amastigotes in Group I biopsies were detected by routine histopathological exam (30.2%), imprint (28.2%), culture (43.4%), immunofluorescence (41.4%) and immunoperoxidase (58.5%) techniques; and by the five methods together (79.3%). In Group II, 5.7% of cultures were positive. Leishmanial antigen was also seen in the cytoplasm of macrophages and giant cells (cellular pattern), vessel walls (vascular pattern) and dermal nerves (neural pattern). Positive reaction was detected in 49 (92.5%), 20 (57%) and 4 (67%) biopsies of Groups I, II and III, respectively. Antigen persistency in cicatricial tissue may be related to immunoprotection or on the contrary, to the development of late lesions. We suggest that the cellular, vascular and neural patterns could be applied in the immunodiagnosis of active and cicatricial lesions in which leishmaniasis is suspected.
引用
收藏
页码:987 / 996
页数:10
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