| Autor: |
Knudson CJ; Department of Microbiology and Immunology, Thomas Jefferson Universitygrid.265008.9, Philadelphia, Pennsylvania, USA., Férez M; Department of Microbiology and Immunology, Thomas Jefferson Universitygrid.265008.9, Philadelphia, Pennsylvania, USA., Alves-Peixoto P; Department of Microbiology and Immunology, Thomas Jefferson Universitygrid.265008.9, Philadelphia, Pennsylvania, USA.; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal.; ICVS/3B's-PT Government Associate Laboratory, Braga/Guimarães, Portugal., Erkes DA; Department of Microbiology and Immunology, Thomas Jefferson Universitygrid.265008.9, Philadelphia, Pennsylvania, USA., Melo-Silva CR; Department of Microbiology and Immunology, Thomas Jefferson Universitygrid.265008.9, Philadelphia, Pennsylvania, USA., Tang L; Department of Microbiology and Immunology, Thomas Jefferson Universitygrid.265008.9, Philadelphia, Pennsylvania, USA., Snyder CM; Department of Microbiology and Immunology, Thomas Jefferson Universitygrid.265008.9, Philadelphia, Pennsylvania, USA., Sigal LJ; Department of Microbiology and Immunology, Thomas Jefferson Universitygrid.265008.9, Philadelphia, Pennsylvania, USA. |
| Abstrakt: |
Cytotoxic CD4 T lymphocytes (CD4-CTL) are important in antiviral immunity. For example, we have previously shown that in mice, CD4-CTL are important to control ectromelia virus (ECTV) infection. How viral infections induce CD4-CTL responses remains incompletely understood. We demonstrate here that not only ECTV but also vaccinia virus and lymphocytic choriomeningitis virus induce CD4-CTL, though the response to ECTV is stronger. Using ECTV, we also demonstrate that in contrast to CD8-CTL, CD4-CTL differentiation requires constant virus replication and ceases once the virus is controlled. We also show that major histocompatibility complex class II molecules on CD11c + cells are required for CD4-CTL differentiation and for mousepox resistance. Transcriptional analysis indicated that antiviral CD4-CTL and noncytolytic T helper 1 (Th1) CD4 T cells have similar transcriptional profiles, suggesting that CD4-CTL are terminally differentiated classical Th1 cells. Interestingly, CD4-CTL and classical Th1 cells expressed similar mRNA levels of the transcription factors ThPOK and GATA-3, necessary for CD4 T cell linage commitment, and Runx3, required for CD8 T cell development and effector function. However, at the protein level, CD4-CTL had higher levels of the three transcription factors, suggesting that further posttranscriptional regulation is required for CD4-CTL differentiation. Finally, CRISPR/Cas9-mediated deletion of Runx3 in CD4 T cells inhibited CD4-CTL but not classical Th1 cell differentiation in response to ECTV infection. These results further our understanding of the mechanisms of CD4-CTL differentiation during viral infection and the role of posttranscriptionally regulated Runx3 in this process. IMPORTANCE While it is well established that cytotoxic CD4 T cells (CD4-CTLs) directly contribute to viral clearance, it remains unclear how CD4-CTL are induced. We now show that CD4-CTLs require sustained antigen presentation and are induced by CD11c-expressing antigen-presenting cells. Moreover, we show that CD4-CTLs are derived from the terminal differentiation of classical T helper 1 (Th1) subset of CD4 cells. Compared to Th1 cells, CD4-CTLs upregulate protein levels of the transcription factors ThPOK, Runx3, and GATA-3 posttranscriptionally. Deletion of Runx3 in differentiated CD4 T cells prevents induction of CD4-CTLs but not classical Th1 cells. These results advance our knowledge of how CD4-CTLs are induced during viral infection. |
