MENGENAI EPISOD INI
Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2020.07.30.227470v1?rss=1
Authors: Bos, R., Rutten, L., van der Lubbe, J. E. M., Bakkers, M. J. G., Hardenberg, G., Wegmann, F., Zuijdgeest, D., de Wilde, A. H., Koornneef, A., Verwilligen, A., van Manen, D., Kwaks, T., Vogels, R., Dalebout, T. J., Myeni, S. K., Kikkert, M., Snijder, E. J., Li, Z., Barouch, D. H., Jort, V., Langedijk, J. P., Zahn, R. C., Custers, J., Schuitemaker, H.
Abstract:
Development of effective preventative interventions against SARS-CoV-2, the etiologic agent of COVID-19 is urgently needed. The viral surface spike (S) protein of SARS-CoV-2 is a key target for prophylactic measures as it is critical for the viral replication cycle and the primary target of neutralizing antibodies. We evaluated design elements previously shown for other coronavirus S protein-based vaccines to be successful, e.g. prefusion-stabilizing substitutions and heterologous signal peptides, for selection of a S-based SARS-CoV-2 vaccine candidate. In vitro characterization demonstrated that the introduction of stabilizing substitutions (i.e., furin cleavage site mutations and two consecutive prolines in the hinge region of S1) increased the ratio of neutralizing versus non-neutralizing antibody binding, suggestive for a prefusion conformation of the S protein. Furthermore, the wild type signal peptide was best suited for the correct cleavage needed for a natively-folded protein. These observations translated into superior immunogenicity in mice where the Ad26 vector encoding for a membrane-bound stabilized S protein with a wild type signal peptide elicited potent neutralizing humoral immunity and cellular immunity that was polarized towards Th1 IFN-{gamma}. This optimized Ad26 vector-based vaccine for SARS-CoV-2, termed Ad26.COV2.S, is currently being evaluated in a phase I clinical trial (ClinicalTrials.gov Identifier: NCT04436276).
Copy rights belong to original authors. Visit the link for more info
http://biorxiv.org/cgi/content/short/2020.07.30.227470v1?rss=1
Authors: Bos, R., Rutten, L., van der Lubbe, J. E. M., Bakkers, M. J. G., Hardenberg, G., Wegmann, F., Zuijdgeest, D., de Wilde, A. H., Koornneef, A., Verwilligen, A., van Manen, D., Kwaks, T., Vogels, R., Dalebout, T. J., Myeni, S. K., Kikkert, M., Snijder, E. J., Li, Z., Barouch, D. H., Jort, V., Langedijk, J. P., Zahn, R. C., Custers, J., Schuitemaker, H.
Abstract:
Development of effective preventative interventions against SARS-CoV-2, the etiologic agent of COVID-19 is urgently needed. The viral surface spike (S) protein of SARS-CoV-2 is a key target for prophylactic measures as it is critical for the viral replication cycle and the primary target of neutralizing antibodies. We evaluated design elements previously shown for other coronavirus S protein-based vaccines to be successful, e.g. prefusion-stabilizing substitutions and heterologous signal peptides, for selection of a S-based SARS-CoV-2 vaccine candidate. In vitro characterization demonstrated that the introduction of stabilizing substitutions (i.e., furin cleavage site mutations and two consecutive prolines in the hinge region of S1) increased the ratio of neutralizing versus non-neutralizing antibody binding, suggestive for a prefusion conformation of the S protein. Furthermore, the wild type signal peptide was best suited for the correct cleavage needed for a natively-folded protein. These observations translated into superior immunogenicity in mice where the Ad26 vector encoding for a membrane-bound stabilized S protein with a wild type signal peptide elicited potent neutralizing humoral immunity and cellular immunity that was polarized towards Th1 IFN-{gamma}. This optimized Ad26 vector-based vaccine for SARS-CoV-2, termed Ad26.COV2.S, is currently being evaluated in a phase I clinical trial (ClinicalTrials.gov Identifier: NCT04436276).
Copy rights belong to original authors. Visit the link for more info
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EPISOD LAIN DALAM PODCAST INI
Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2020.08.12.247510v1?rss=1
Authors: Agerholm, R., Rizk, J., Kadekar, D., Borch, A., Hadrup, S. R., Bekiaris, V.
Abstract:
The vitamin A metabolite retinoic acid (RA) and its receptor (RAR) are one of the key interactions regulating c ...
Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2020.08.12.248252v1?rss=1
Authors: Kiritsy, M. C., Ankley, L. M., Trombley, J. D., Huizinga, G. P., Lord, A. E., Orning, P., Elling, R., Fitzgerald, K. A., Olive, A.
Abstract:
Cytokine-mediated activation of host immunity is central ...
Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2020.08.12.248021v1?rss=1
Authors: Noon, J. B., Sharma, A., Platten, J., Quinton, L. J., Reinhardt, C., Bosmann, M.
Abstract:
Interleukin-27 (IL-27) is a heterodimeric cytokine of the IL-12 family, formed by non-covalent association ...
Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2020.08.11.247395v1?rss=1
Authors: Walls, A. C., Fiala, B., Schaefer, A., Wrenn, S., Pham, M. N., Murphy, M., Tse, L. V., Shehata, L., O'Connor, M. A., Chen, C., Navarro, M. J., Miranda, M. C., Pettie, D., Ravichandran, R., Kraft, J. ...
Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2020.08.12.247965v1?rss=1
Authors: Vincent, C. M., Dionne, M. S.
Abstract:
Male and female animals exhibit differences in infection outcomes. One possible source of sexually dimorphic immunity is sex-specific costs of immune activit ...
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