G. Lima

发表

Macrophages at intermediate stage of maturation produce high levels of IL-12 p40 upon stimulation with Leishmania.

P. Leenen, C. Tadokoro, L. Vieira, 2005, Microbes and infection.

Leishmania spp. parasite isolation through inoculation of patient biopsy macerates in interferon gamma knockout mice.

S. A. Pinto, L. I. A. Pereira, M. Dorta, 2010, Revista do Instituto de Medicina Tropical de Sao Paulo.

T-cell compartment involvement in two high antibody responder lines of mice (HI and HII Biozzi mice) respectively susceptible and resistant to collagen-induced arthritis.

J. Couderc, J. Mével, G. Lima, 1993, Journal of autoimmunity.

Murine T-cell responses to protozoan and metazoan parasites: functional analysis of T-cell lines and clones specific for Leishmania tropica and Schistosoma mansoni.

R. Titus, J. Louis, G. Lima, 1984, Contemporary topics in immunobiology.

The in vitro Generation and Functional Analysis of Murine T Cell Populations and Clones Specific for a Protozoan Parasite, Leishmania tropica

R. Zubler, J. Louis, H. Engers, 1982, Immunological reviews.

Immature macrophages derived from mouse bone marrow produce large amounts of IL‐12p40 after LPS stimulation

P. Leenen, M. A. Oliveira, I. Abrahamsohn, 2003, Journal of leukocyte biology.

Exacerbation of murine cutaneous leishmaniasis by adoptive transfer of parasite-specific helper T cell populations capable of mediating Leishmania major-specific delayed-type hypersensitivity.

R. Titus, J. Louis, H. Engers, 1984, Journal of immunology.

Adoptive transfer of delayed type hypersensitivity reactions specific for Leishmania major antigens to normal mice using murine T cell populations and clones generated in vitro.

J. Louis, H. Engers, G. Lima, 1984, Clinical and experimental immunology.

Leishmania (Leishmania) amazonensis infection and dissemination in mice inoculated with stationary-phase or with purified metacyclic promastigotes

T. Felizardo, L. Toma, G. Lima, 2007, Parasitology.

Antibody suppression in mice infected with Nippostrongylus brasiliensis

I. Mota, D. Haig, G. Lima, 1980, Parasite immunology.

Increase of NK cells and proinflammatory monocytes are associated with the clinical improvement of diffuse cutaneous leishmaniasis after immunochemotherapy with BCG/Leishmania antigens.

V. Toledo, W. Mayrink, S. A. Pinto, 2009, The American journal of tropical medicine and hygiene.

Lack of signaling by IL-4 or by IL-4/IL-13 has more attenuating effects on Leishmania amazonensis dorsal skin--than on footpad-infected mice.

T. Felizardo, M. I. Gaspar-Elsas, G. Lima, 2012, Experimental parasitology.

Identification and Biological Characterization of Leishmania (Viannia) guyanensis Isolated from a Patient with Tegumentary Leishmaniasis in Goiás, a Nonendemic Area for This Species in Brazil

S. R. Uliana, S. A. Pinto, R. S. L. Lino Júnior, 2015, BioMed research international.

Antigen-specific Il-4- and IL-10-secreting CD4+ lymphocytes increase in vivo susceptibility to Trypanosoma cruzi infection.

M. Lafaille, G. Lima, I. Abrahamsohn, 1996 .

Murine T Lymphocyte Responses Specific for the Protozoan Parasites Leishmania tropica and Trypanosoma brucei

J. Louis, H. Engers, G. Lima, 1982, Clinics in Immunology and Allergy.

Trypanosoma cruzi: maintenance of parasite-specific T cell responses in lymph nodes during the acute phase of the infection.

M. A. Curotto de Lafaille, G. Lima, I. Abrahamsohn, 1990, Experimental parasitology.