Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117
Cohen, Y. Z., Lorenzi, J. C. C., Krassnig, L., Barton, J. P., Burke, L., Pai, J., Lu, C.-L., Mendoza, P., Oliveira, T. Y., Sleckman, C., Millard, K., Butler, A. L., Dizon, J. P., Belblidia, S. A., Witmer-Pack, M., Shimeliovich, I., Gulick, R. M., Seaman, M. S., Jankovic, M., Caskey, M., Nussenzweig, M. C.
Rockefeller University Press
Published 2018
Rockefeller University Press
Published 2018
Publication Date: |
2018-09-04
|
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Publisher: |
Rockefeller University Press
|
Print ISSN: |
0022-1007
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Electronic ISSN: |
1540-9538
|
Topics: |
Medicine
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Keywords: |
Infectious Disease and Host Defense
|
Published by: |
_version_ | 1836399042439938049 |
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autor | Cohen, Y. Z., Lorenzi, J. C. C., Krassnig, L., Barton, J. P., Burke, L., Pai, J., Lu, C.-L., Mendoza, P., Oliveira, T. Y., Sleckman, C., Millard, K., Butler, A. L., Dizon, J. P., Belblidia, S. A., Witmer-Pack, M., Shimeliovich, I., Gulick, R. M., Seaman, M. S., Jankovic, M., Caskey, M., Nussenzweig, M. C. |
beschreibung | A clinical trial was performed to evaluate 3BNC117, a potent anti–HIV-1 antibody, in infected individuals during suppressive antiretroviral therapy and subsequent analytical treatment interruption (ATI). The circulating reservoir was evaluated by quantitative and qualitative viral outgrowth assay (Q 2 VOA) at entry and after 6 mo. There were no significant quantitative changes in the size of the reservoir before ATI, and the composition of circulating reservoir clones varied in a manner that did not correlate with 3BNC117 sensitivity. 3BNC117 binding site amino acid variants found in rebound viruses preexisted in the latent reservoir. However, only 3 of 217 rebound viruses were identical to 868 latent viruses isolated by Q 2 VOA and near full-length sequencing. Instead, 63% of the rebound viruses appeared to be recombinants, even in individuals with 3BNC117-resistant reservoir viruses. In conclusion, viruses emerging during ATI in individuals treated with 3BNC117 are not the dominant species found in the circulating latent reservoir, but frequently appear to represent recombinants of latent viruses. |
citation_standardnr | 6327530 |
datenlieferant | ipn_articles |
feed_id | 96 |
feed_publisher | Rockefeller University Press |
feed_publisher_url | http://www.rupress.org/ |
insertion_date | 2018-09-04 |
journaleissn | 1540-9538 |
journalissn | 0022-1007 |
publikationsjahr_anzeige | 2018 |
publikationsjahr_facette | 2018 |
publikationsjahr_intervall | 7984:2015-2019 |
publikationsjahr_sort | 2018 |
publisher | Rockefeller University Press |
quelle | Journal of Experimental Medicine |
relation | http://jem.rupress.org/cgi/content/short/215/9/2311?rss=1 |
schlagwort | Infectious Disease and Host Defense |
search_space | articles |
shingle_author_1 | Cohen, Y. Z., Lorenzi, J. C. C., Krassnig, L., Barton, J. P., Burke, L., Pai, J., Lu, C.-L., Mendoza, P., Oliveira, T. Y., Sleckman, C., Millard, K., Butler, A. L., Dizon, J. P., Belblidia, S. A., Witmer-Pack, M., Shimeliovich, I., Gulick, R. M., Seaman, M. S., Jankovic, M., Caskey, M., Nussenzweig, M. C. |
shingle_author_2 | Cohen, Y. Z., Lorenzi, J. C. C., Krassnig, L., Barton, J. P., Burke, L., Pai, J., Lu, C.-L., Mendoza, P., Oliveira, T. Y., Sleckman, C., Millard, K., Butler, A. L., Dizon, J. P., Belblidia, S. A., Witmer-Pack, M., Shimeliovich, I., Gulick, R. M., Seaman, M. S., Jankovic, M., Caskey, M., Nussenzweig, M. C. |
shingle_author_3 | Cohen, Y. Z., Lorenzi, J. C. C., Krassnig, L., Barton, J. P., Burke, L., Pai, J., Lu, C.-L., Mendoza, P., Oliveira, T. Y., Sleckman, C., Millard, K., Butler, A. L., Dizon, J. P., Belblidia, S. A., Witmer-Pack, M., Shimeliovich, I., Gulick, R. M., Seaman, M. S., Jankovic, M., Caskey, M., Nussenzweig, M. C. |
shingle_author_4 | Cohen, Y. Z., Lorenzi, J. C. C., Krassnig, L., Barton, J. P., Burke, L., Pai, J., Lu, C.-L., Mendoza, P., Oliveira, T. Y., Sleckman, C., Millard, K., Butler, A. L., Dizon, J. P., Belblidia, S. A., Witmer-Pack, M., Shimeliovich, I., Gulick, R. M., Seaman, M. S., Jankovic, M., Caskey, M., Nussenzweig, M. C. |
shingle_catch_all_1 | Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117 Infectious Disease and Host Defense A clinical trial was performed to evaluate 3BNC117, a potent anti–HIV-1 antibody, in infected individuals during suppressive antiretroviral therapy and subsequent analytical treatment interruption (ATI). The circulating reservoir was evaluated by quantitative and qualitative viral outgrowth assay (Q 2 VOA) at entry and after 6 mo. There were no significant quantitative changes in the size of the reservoir before ATI, and the composition of circulating reservoir clones varied in a manner that did not correlate with 3BNC117 sensitivity. 3BNC117 binding site amino acid variants found in rebound viruses preexisted in the latent reservoir. However, only 3 of 217 rebound viruses were identical to 868 latent viruses isolated by Q 2 VOA and near full-length sequencing. Instead, 63% of the rebound viruses appeared to be recombinants, even in individuals with 3BNC117-resistant reservoir viruses. In conclusion, viruses emerging during ATI in individuals treated with 3BNC117 are not the dominant species found in the circulating latent reservoir, but frequently appear to represent recombinants of latent viruses. Cohen, Y. Z., Lorenzi, J. C. C., Krassnig, L., Barton, J. P., Burke, L., Pai, J., Lu, C.-L., Mendoza, P., Oliveira, T. Y., Sleckman, C., Millard, K., Butler, A. L., Dizon, J. P., Belblidia, S. A., Witmer-Pack, M., Shimeliovich, I., Gulick, R. M., Seaman, M. S., Jankovic, M., Caskey, M., Nussenzweig, M. C. Rockefeller University Press 0022-1007 00221007 1540-9538 15409538 |
shingle_catch_all_2 | Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117 Infectious Disease and Host Defense A clinical trial was performed to evaluate 3BNC117, a potent anti–HIV-1 antibody, in infected individuals during suppressive antiretroviral therapy and subsequent analytical treatment interruption (ATI). The circulating reservoir was evaluated by quantitative and qualitative viral outgrowth assay (Q 2 VOA) at entry and after 6 mo. There were no significant quantitative changes in the size of the reservoir before ATI, and the composition of circulating reservoir clones varied in a manner that did not correlate with 3BNC117 sensitivity. 3BNC117 binding site amino acid variants found in rebound viruses preexisted in the latent reservoir. However, only 3 of 217 rebound viruses were identical to 868 latent viruses isolated by Q 2 VOA and near full-length sequencing. Instead, 63% of the rebound viruses appeared to be recombinants, even in individuals with 3BNC117-resistant reservoir viruses. In conclusion, viruses emerging during ATI in individuals treated with 3BNC117 are not the dominant species found in the circulating latent reservoir, but frequently appear to represent recombinants of latent viruses. Cohen, Y. Z., Lorenzi, J. C. C., Krassnig, L., Barton, J. P., Burke, L., Pai, J., Lu, C.-L., Mendoza, P., Oliveira, T. Y., Sleckman, C., Millard, K., Butler, A. L., Dizon, J. P., Belblidia, S. A., Witmer-Pack, M., Shimeliovich, I., Gulick, R. M., Seaman, M. S., Jankovic, M., Caskey, M., Nussenzweig, M. C. Rockefeller University Press 0022-1007 00221007 1540-9538 15409538 |
shingle_catch_all_3 | Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117 Infectious Disease and Host Defense A clinical trial was performed to evaluate 3BNC117, a potent anti–HIV-1 antibody, in infected individuals during suppressive antiretroviral therapy and subsequent analytical treatment interruption (ATI). The circulating reservoir was evaluated by quantitative and qualitative viral outgrowth assay (Q 2 VOA) at entry and after 6 mo. There were no significant quantitative changes in the size of the reservoir before ATI, and the composition of circulating reservoir clones varied in a manner that did not correlate with 3BNC117 sensitivity. 3BNC117 binding site amino acid variants found in rebound viruses preexisted in the latent reservoir. However, only 3 of 217 rebound viruses were identical to 868 latent viruses isolated by Q 2 VOA and near full-length sequencing. Instead, 63% of the rebound viruses appeared to be recombinants, even in individuals with 3BNC117-resistant reservoir viruses. In conclusion, viruses emerging during ATI in individuals treated with 3BNC117 are not the dominant species found in the circulating latent reservoir, but frequently appear to represent recombinants of latent viruses. Cohen, Y. Z., Lorenzi, J. C. C., Krassnig, L., Barton, J. P., Burke, L., Pai, J., Lu, C.-L., Mendoza, P., Oliveira, T. Y., Sleckman, C., Millard, K., Butler, A. L., Dizon, J. P., Belblidia, S. A., Witmer-Pack, M., Shimeliovich, I., Gulick, R. M., Seaman, M. S., Jankovic, M., Caskey, M., Nussenzweig, M. C. Rockefeller University Press 0022-1007 00221007 1540-9538 15409538 |
shingle_catch_all_4 | Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117 Infectious Disease and Host Defense A clinical trial was performed to evaluate 3BNC117, a potent anti–HIV-1 antibody, in infected individuals during suppressive antiretroviral therapy and subsequent analytical treatment interruption (ATI). The circulating reservoir was evaluated by quantitative and qualitative viral outgrowth assay (Q 2 VOA) at entry and after 6 mo. There were no significant quantitative changes in the size of the reservoir before ATI, and the composition of circulating reservoir clones varied in a manner that did not correlate with 3BNC117 sensitivity. 3BNC117 binding site amino acid variants found in rebound viruses preexisted in the latent reservoir. However, only 3 of 217 rebound viruses were identical to 868 latent viruses isolated by Q 2 VOA and near full-length sequencing. Instead, 63% of the rebound viruses appeared to be recombinants, even in individuals with 3BNC117-resistant reservoir viruses. In conclusion, viruses emerging during ATI in individuals treated with 3BNC117 are not the dominant species found in the circulating latent reservoir, but frequently appear to represent recombinants of latent viruses. Cohen, Y. Z., Lorenzi, J. C. C., Krassnig, L., Barton, J. P., Burke, L., Pai, J., Lu, C.-L., Mendoza, P., Oliveira, T. Y., Sleckman, C., Millard, K., Butler, A. L., Dizon, J. P., Belblidia, S. A., Witmer-Pack, M., Shimeliovich, I., Gulick, R. M., Seaman, M. S., Jankovic, M., Caskey, M., Nussenzweig, M. C. Rockefeller University Press 0022-1007 00221007 1540-9538 15409538 |
shingle_title_1 | Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117 |
shingle_title_2 | Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117 |
shingle_title_3 | Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117 |
shingle_title_4 | Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117 |
timestamp | 2025-06-30T23:36:41.168Z |
titel | Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117 |
titel_suche | Relationship between latent and rebound viruses in a clinical trial of anti-HIV-1 antibody 3BNC117 |
topic | WW-YZ |
uid | ipn_articles_6327530 |