collection
https://read.qxmd.com/read/27620712/lung-cancer-first-line-immunotherapy-in-lung-cancer-taking-the-first-step
#21
COMMENT
Stephen V Liu, Giuseppe Giaccone
No abstract text is available yet for this article.
October 2016: Nature Reviews. Clinical Oncology
https://read.qxmd.com/read/27664133/targeting-immune-checkpoints-in-hematologic-malignancies
#22
REVIEW
Gheath Alatrash, Naval Daver, Elizabeth A Mittendorf
The use of antibodies that target immune checkpoint molecules on the surface of T-lymphocytes and/or tumor cells has revolutionized our approach to cancer therapy. Cytotoxic-T-lymphocyte antigen (CTLA-4) and programmed cell death protein 1 (PD-1) are the two most commonly targeted immune checkpoint molecules. Although the role of antibodies that target CTLA-4 and PD-1 has been established in solid tumor malignancies and Food and Drug Administration approved for melanoma and non-small cell lung cancer, there remains a desperate need to incorporate immune checkpoint inhibition in hematologic malignancies...
October 2016: Pharmacological Reviews
https://read.qxmd.com/read/27448784/novel-approaches-in-cancer-immunotherapy-a-light-at-the-end-of-the-tunnel
#23
JOURNAL ARTICLE
Monika Joshi, Sumanta K Pal, Joseph J Drabick
After decades of disappointments, the use of immunotherapy in cancer has finally come of age and resulted in a real paradigm shift in cancer treatment across many tumor types. With the advent of novel immunotherapies based on increasing understanding of the human immune system, cure has become a real possibility for many patients. The development of cancer vaccines, immune checkpoint inhibitors, chimeric antigen receptor T cell, oncolytic virus based immunotherapy to name a few have given hope to patients. One of the most exciting developments in the era of immunotherapy has been the discovery of checkpoint inhibitors causing blockade of two important immune pathways -- cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and programmed death receptor-1 (PD-1), resulting in empowerment of anti-tumor immunity...
June 2016: Discovery Medicine
https://read.qxmd.com/read/26599172/cancer-immunotherapy-researchers-focus-on-refining-checkpoint-blockade-therapies
#24
Julie A Jacob
No abstract text is available yet for this article.
November 24, 2015: JAMA
https://read.qxmd.com/read/27365430/immunology-fighting-autoimmunity-with-immune-cells
#25
Mitch Leslie
No abstract text is available yet for this article.
July 1, 2016: Science
https://read.qxmd.com/read/26977783/immunotherapy-pd-1-says-goodbye-tim-3-says-hello
#26
COMMENT
Diana Romero
No abstract text is available yet for this article.
April 2016: Nature Reviews. Clinical Oncology
https://read.qxmd.com/read/26541610/anticancer-immunotherapy-by-ctla-4-blockade-relies-on-the-gut-microbiota
#27
JOURNAL ARTICLE
Marie Vétizou, Jonathan M Pitt, Romain Daillère, Patricia Lepage, Nadine Waldschmitt, Caroline Flament, Sylvie Rusakiewicz, Bertrand Routy, Maria P Roberti, Connie P M Duong, Vichnou Poirier-Colame, Antoine Roux, Sonia Becharef, Silvia Formenti, Encouse Golden, Sascha Cording, Gerard Eberl, Andreas Schlitzer, Florent Ginhoux, Sridhar Mani, Takahiro Yamazaki, Nicolas Jacquelot, David P Enot, Marion Bérard, Jérôme Nigou, Paule Opolon, Alexander Eggermont, Paul-Louis Woerther, Elisabeth Chachaty, Nathalie Chaput, Caroline Robert, Christina Mateus, Guido Kroemer, Didier Raoult, Ivo Gomperts Boneca, Franck Carbonnel, Mathias Chamaillard, Laurence Zitvogel
Antibodies targeting CTLA-4 have been successfully used as cancer immunotherapy. We find that the antitumor effects of CTLA-4 blockade depend on distinct Bacteroides species. In mice and patients, T cell responses specific for B. thetaiotaomicron or B. fragilis were associated with the efficacy of CTLA-4 blockade. Tumors in antibiotic-treated or germ-free mice did not respond to CTLA blockade. This defect was overcome by gavage with B. fragilis, by immunization with B. fragilis polysaccharides, or by adoptive transfer of B...
November 27, 2015: Science
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