In vivo treatment with ril-12 protects susceptible mice from Paracoccidioides brasiliensis pulmonary infection whereas in vivo neutralization of il-4 does not alter disease outcome (1996)
- Autores:
- Autores USP: CALICH, VERA LUCIA GARCIA - ICB ; KASHINO, SUELY SANAE - ICB ; RUSSO, MOMTCHILO - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Resumos
- Nome do evento: Congresso do Instituto de Ciências Biomédicas da Universidade de São Paulo
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ABNT
ARRUDA, C et al. In vivo treatment with ril-12 protects susceptible mice from Paracoccidioides brasiliensis pulmonary infection whereas in vivo neutralization of il-4 does not alter disease outcome. 1996, Anais.. São Paulo: ICB-USP, 1996. . Acesso em: 18 abr. 2024. -
APA
Arruda, C., Fazioli, R. A., Kashino, S. S., Nascimento, F. R. F., Costa, A. T., Russo, M., & Calich, V. L. G. (1996). In vivo treatment with ril-12 protects susceptible mice from Paracoccidioides brasiliensis pulmonary infection whereas in vivo neutralization of il-4 does not alter disease outcome. In Resumos. São Paulo: ICB-USP. -
NLM
Arruda C, Fazioli RA, Kashino SS, Nascimento FRF, Costa AT, Russo M, Calich VLG. In vivo treatment with ril-12 protects susceptible mice from Paracoccidioides brasiliensis pulmonary infection whereas in vivo neutralization of il-4 does not alter disease outcome. Resumos. 1996 ;[citado 2024 abr. 18 ] -
Vancouver
Arruda C, Fazioli RA, Kashino SS, Nascimento FRF, Costa AT, Russo M, Calich VLG. In vivo treatment with ril-12 protects susceptible mice from Paracoccidioides brasiliensis pulmonary infection whereas in vivo neutralization of il-4 does not alter disease outcome. Resumos. 1996 ;[citado 2024 abr. 18 ] - Cytokines production (il-2, ifn-'GAMA', il-4, il-10) in the protection and exacerbation models of murine experimental paracoccidioidomycosis
- Cytokines production (il-2, ifn-gama, il-4, il-10) in the protection and exacerbation models of murine experimental paracoccidioidomycosis
- Characterization of lymphoproliferative response and type 1 and type 2 cytokines during infection of resistant and susceptible mice with paracoccidioides brasiliensis
- Characterization of lymphoproliferative responses and type 1 and type 2 cytokines production during infection of resistant and susceptible mice with paracoccidioides brasiliensis
- In vivo treatment with ril-12 protects susceptible mice from Paracoccidioides brasiliensis infection whereas in vivo neutralization of il-4 does not alter disease outcome
- Dual role for nitric oxide in paracoccidioidomycosis: Essential for resistance, but overproduction associated with susceptibility
- Polyclonal activation of B lymphocytes in experimental murine paracoccidioidomycosis
- T-cell control of inflammatory and macrophage responses induced by injection of con a in mice
- Experimental murine paracoccidioidomycosis: immune and non immune responses vary according to mice susceptibility and fungi virulence
- In vivo treatment with r-IL12 protects susceptible mice from Paracoccidioides brasiliensis pulmonary infection whereas in vivo neutralization of IL-4 does not alter disease outcome
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