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                  <mods:namePart>Martinez-Lopez, Maria</mods:namePart>
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               <mods:identifier type="citation">Eur J Immunol. 2015; 45(1):119-29</mods:identifier>
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               <mods:identifier type="e-issn">1521-4141</mods:identifier>
               <mods:identifier type="issn">0014-2980</mods:identifier>
               <mods:identifier type="journal">European Journal of Immunology</mods:identifier>
               <mods:identifier type="pubmedID">25312824</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/5526</mods:identifier>
               <mods:abstract>The role of different DC subsets in priming and maintenance of immunity against Leishmania major (L. major) infection is debated. The transcription factor basic leucine zipper transcription factor, ATF-like 3 (Batf3) is essential for the development of mouse CD103(+) DCs and some functions of CD8(+) DCs. We found that CD103(+) DCs were significantly reduced in the dermis of Batf3-deficient C57BL/6 mice. Batf3(-/-) mice developed exacerbated and unresolved cutaneous pathology following a low dose of intradermal L. major infection in the ear pinnae. Parasite load was increased 1000-fold locally and expanded systemically. Batf3 deficiency did not affect L. major antigen presentation to T cells, which was directly exerted by CD8(-) conventional DCs (cDCs) in the skin draining LN. However, CD4(+) T-cell differentiation in the LN and skin was skewed to nonprotective Treg- and Th2-cell subtypes. CD103(+) DCs are major IL-12 producers during L. major infection. Local Th1 immunity was severely hindered, correlating with impaired IL-12 production and reduction in CD103(+) DC numbers. Adoptive transfer of WT but not IL-12p40(-/-) Batf3-dependent DCs significantly improved anti-L. major response in infected Batf3(-/-) mice. Our results suggest that IL-12 production by Batf3-dependent CD103(+) DCs is crucial for maintenance of local Th1 immunity against L. major infection.</mods:abstract>
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               <mods:subject>
                  <mods:topic>Adaptive immune response</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Batf3</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Dendritic cells</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>IL-12</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Leishmania major</mods:topic>
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               <mods:subject>
                  <mods:topic>T-CELLS</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>CROSS-PRESENTATION</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>LANGERHANS CELLS</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>CUTTING EDGE</mods:topic>
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               <mods:subject>
                  <mods:topic>IN-VIVO</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>RESPONSES</mods:topic>
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               <mods:subject>
                  <mods:topic>SKIN</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>CD8(+)</mods:topic>
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                  <mods:topic>INTERLEUKIN-12</mods:topic>
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                  <mods:title>Batf3-dependent CD103(+) dendritic cells are major producers of IL-12 that drive local Th1 immunity against Leishmania major infection in mice</mods:title>
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