His primary areas of investigation include Immunology, Leishmania major, Molecular biology, Interleukin 4 and BALB/c. His work focuses on many connections between Immunology and other disciplines, such as Cytotoxic T cell, that overlap with his field of interest in T cell. His Leishmania major research is multidisciplinary, relying on both Immune system and Lymph node.
His work in Molecular biology addresses subjects such as Virology, which are connected to disciplines such as Interferon gamma and CD1D. His Interleukin 4 research includes elements of IL-2 receptor, Cell growth, Spleen transplantation, Messenger RNA and Interleukin 12. He has researched BALB/c in several fields, including Regulatory T cell, Spleen and Adoptive cell transfer.
Jacques A. Louis mostly deals with Immunology, Leishmania major, Molecular biology, T cell and Antigen. His study brings together the fields of In vivo and Immunology. His Leishmania major study incorporates themes from Tumor necrosis factor alpha, Cytokine, Cell growth and BALB/c.
His work carried out in the field of Molecular biology brings together such families of science as Virology, Ratón, Spleen, Interleukin 4 and T-cell receptor. His Virology research incorporates themes from CD5, Antibody, Adoptive cell transfer and CD8. His biological study spans a wide range of topics, including Cytotoxic T cell, In vitro and Leishmania tropica.
Jacques A. Louis focuses on Leishmania major, Molecular biology, Immunology, Pathogenesis and Cell growth. His studies in Leishmania major integrate themes in fields like Cellular differentiation and Cell biology. The Molecular biology study combines topics in areas such as Adoptive cell transfer, Virology, Cytokine and BALB/c.
Much of his study explores Immunology relationship to Histamine. His Cell growth research is multidisciplinary, incorporating perspectives in Neutralization, Ratón, Interleukin 4 and Epitope, Epitope mapping. His Plasmodium berghei research incorporates elements of Immune system and Microbiology.
Immunology, Interleukin 10, CD5, Naive B cell and Regulatory B cells are his primary areas of study. He brings together Immunology and Histamine binding to produce work in his papers. The concepts of his Interleukin 10 study are interwoven with issues in B-1 cell, BALB/c, CD1D, Molecular biology and Adoptive cell transfer.
Many of his studies on CD5 involve topics that are commonly interrelated, such as Virology.
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Genetically resistant mice lacking interleukin-12 are susceptible to infection with Leishmania major and mount a polarized Th2 cell response.
Frank Mattner;Jeanne Magram;Jessica Ferrante;Pascal Launois.
European Journal of Immunology (1996)
Natural Killer Cells Activated by MHC Class ILow Targets Prime Dendritic Cells to Induce Protective CD8 T Cell Responses
Ralph Mocikat;Heidi Braumüller;Heidi Braumüller;Alain Gumy;Oliver Egeter.
IL-4 Rapidly Produced by Vβ4 Vα8 CD4+ T Cells Instructs Th2 Development and Susceptibility to Leishmania major in BALB/c Mice
Pascal Launois;Ivan Maillard;Sabine Pingel;Kristin G. Swihart.
IL-4 instructs TH1 responses and resistance to Leishmania major in susceptible BALB/c mice.
Tilo Biedermann;Stephan Zimmermann;Stephan Zimmermann;Hayo Himmelrich;Alain Gumy.
Nature Immunology (2001)
An immunomodulatory function for neutrophils during the induction of a CD4+ Th2 response in BALB/c mice infected with Leishmania major.
Fabienne Tacchini-Cottier;C. Zweifel;Y. Belkaid;C. Mukankundiye.
Journal of Immunology (2000)
Mice from a genetically resistant background lacking the interferon gamma receptor are susceptible to infection with Leishmania major but mount a polarized T helper cell 1-type CD4+ T cell response
K. Swihart;U. Fruth;N. Messmer;K. Hug.
Journal of Experimental Medicine (1995)
L3T4+ T lymphocytes play a major role in the pathogenesis of murine cerebral malaria.
G E Grau;P F Piguet;H D Engers;J A Louis.
Journal of Immunology (1986)
Therapeutic effect of anti-L3T4 monoclonal antibody GK1.5 on cutaneous leishmaniasis in genetically-susceptible BALB/c mice.
R G Titus;R Ceredig;J C Cerottini;J A Louis.
Journal of Immunology (1985)
Mycobacterial heat-shock proteins as carrier molecules. II: The use of the 70-kDa mycobacterial heat-shock protein as carrier for conjugated vaccines can circumvent the need for adjuvants and Bacillus Calmette Guérin priming.
Christy Barrios;Alexander R. Lussow;Jan Van Embden;Ruurd Van Der Zee.
European Journal of Immunology (1992)
Mycobacterial heat-shock proteins as carrier molecules.
A R Lussow;C Barrios;J van Embden;R Van der Zee.
European Journal of Immunology (1991)
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