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DOI: 10.3791/66752-v
Yao Lin*1,2, Shuai Yue*3, Yang Yang*4, Junjian He5, Xiaofan Yang6, Lilin Ye5, Xiangyu Chen7
1Department of Urology, South China Hospital, Medical School,Shenzhen University, 2Guangdong Key Laboratory for Biomedical Measurements and Ultrasound Imaging, National-Regional Key Technology Engineering Laboratory for Medical Ultrasound, School of Biomedical Engineering,Shenzhen University Medical School, 3Cancer Center, Daping Hospital & Army Medical Center of PLA,Third Military Medical University, 4Guangdong Provincial Key Laboratory of Immune Regulation and Immunotherapy, School of Laboratory Medicine and Biotechnology,Southern Medical University, 5Institute of Immunology,Third Military Medical University, 6Dermatology Hospital,Southern Medical University, 7Institute of Immunological Innovation and Translation,Chongqing Medical University
Please note that some of the translations on this page are AI generated. Click here for the English version.
L’étude actuelle présente des protocoles permettant d’évaluer l’engagement précoce du devenir des cellules TFH spécifiques du virus et de manipuler l’expression génique dans ces cellules.
Notre recherche décrit des méthodes reproductibles pour évaluer l’engagement précoce du devenir des cellules TFH spécifiques du virus, y compris l’établissement d’un modèle de souris monoclonale aiguë infectée par le LCMV, la réalisation d’une coloration par cytométrie en flux et la manipulation de gènes basée sur des vecteurs rétroviraux. Par rapport à la stimulation in vitro par cellules T, la stimulation in vivo pourrait activer les cellules T plus rapidement, même en 12 heures, et elle est entièrement activée pour la prochaine transduction du rétrovirus. Nos résultats aideront aux études explorant les mécanismes sous-jacents à l’engagement précoce de diverses cellules TFH spécifiques.
De plus, nos recherches contribueront à comprendre l’immunité humorale dépendante des lymphocytes T et à optimiser la conception des vaccins.
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