Relationship of Heterologous Virus Responses and Outcomes in Hospitalized COVID-19 Patients

IMPACC Network, Yael Rosenberg-Hasson, Tyson H. Holmes, Joann Diray-Arce, Jing Chen, Ryan Kellogg, Michael Snyder, Patrice M. Becker, Al Ozonoff, Nadine Rouphael, Elaine F. Reed, Holden T. Maecker, Ozonoff Al Ozonoff, Joann Diray-Arce, Carly E. Milliren, Kerry McEnaney, Brenda Barton, Claudia Lentucci, Mehmet Saluvan, Ana C. ChangAnnmarie Hoch, Marisa Albert, Tanzia Shaheen, Alvin T. Kho, Shanshan Liu, Sanya Thomas, Jing Chen, Maimouna D. Murphy, Mitchell Cooney, Caitlin Syphurs, Arash Nemati Hayati, Robert Bryant, James Abraham, Joanna Schaenman, Elaine F. Reed, Ramin Salehi-Rad, David Elashoff, Jenny Brook, Estefania Ramires-Sanchez, Megan Llamas, Adreanne Rivera, Claudia Perdomo, Dawn C. Ward, Clara E. Magyar, Jennifer Fulcher, Harry C. Pickering, Subha Sen, Naresh Doni Jayavelu, Matthew C. Altman, Scott Presnell, Bernard Khor, Tomasz Jancsyk, Alejandra Jauregui, Aleksandra Leligdowicz, Alexander Beagle, Alexandra Tsitsiklis, Alyssa Ward, Ana Gonzalez, Andrew W. Schroeder, Andrew Willmore, Arjun Rao, Austin Sigman, Bonny Alvarenga, Bushra Samad, Carolyn Leroux, Carolyn M. Hendrickson, Carolyn S. Calfee, Charles R. Langelier, Christina Love, Cindy Curiel, Cole Shaw, David J. Erle, Deanna Lee, Eran Mick, Gabriela Fragiadakis, Gayelan Tietje-Ulrich, Jayant Rajan, Jeff Milush, Jonathan Singer, Joshua J. Vasquez, Kevin Tangv, Kirsten N. Kangelaris, Legna Betancourt, Lekshmi Santhosh, Lenka Maliskova, Logan Pierce, Luz Torres Altamirano, Maria Tercero Paz, Matthew F. Krummel, Michael Adkisson, Michael Matthay, Michael R. Wilson, Neeta Thakur, Nicklaus Rodriguez, Nicole Sutter, Norman Jones, Pratik Sinha, Prescott G. Woodruff, Priya Prasad, Rajani Ghale, Raphael Lota, Ravi Dandekar, Ravi Patel, Sadeed Rashid, Saurabh Asthana, Sharvari Bhide, Sidney A. Carrillo, Suzanna Chak, Tasha Lea, Viet Nguyen, Walter Eckalbar, Estella Sanchez Guerrero, Yumiko Abe-Jones, Charles B. Cairns, Elias K. Haddad, Mariana Bernui, Debra L. Powell, James N. Kim, Brent Simmons, I. Michael Goonewardene, Cecilia M. Smith, Mark Martens, Michele A. Kutzler, Carolyn Edwards, Jennifer Connors, Edward Lee, Edward Lin, Brett Croen, Nicholas Semenza, Brandon Rogowski, Nataliya Melnyk, Kyra Woloszczuk, Gina Cusimano, Matthew Bell, Sara Furukawa, Renee McLin, Pam Schearer, Julie Sheidy, George P. Tegos, Crystal Nagle, Vicki Seyfert-Margolis, Monica Kraft, Christian Bime, Jarrod Mosier, Hiroki Kimura, Michelle Conway, Dave Francisco, Allyson Molzahn, Heidi Erickson, Connie Cathleen Wilson, Ron Schunk, Trina Hughes, Bianca Sierra, Lindsey R. Baden, Ofer Levy, Kinga K. Smolen, Michael Desjardins, Amy C. Sherman, Stephen R. Walsh, Simon van Haren, Xhoi Mitre, Jessica Cauley, Xiofang Li, Alexandra Tong, Bethany Evans, Christina Montesano, Jose Humberto Licona, Jonathan Krauss, Nicolas C. Issa, Jun Bai Park Chang, Natalie Izaguirre, Hanno Steen, Patrick van Zalm, Benoit Fatou, Kevin Mendez, Jessica Lasky-Su, Meenakshi Jha, Arthur Viode, Rebecca Rooks, Scott R. Hutton, Greg Michelotti, Kari Wong, Albert C. Shaw, Omkar Chaudhary, Andreas Coppi, Charles S. Dela Cruz, Denise Esserman, Shelli Farhadian, John Fournier, David A. Hafler, Akiko Iwasaki, Albert I. Ko, Subhasis Mohanty, Ruth R. Montgomery, M. Catherine Muenker, Allison Nelson, Khadir Raddassi, Michael Rainone, William Ruff, Syim Salahuddin, Wade L. Schulz

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Abstract

The clinical trajectory of COVID-19 may be influenced by previous responses to heterologous viruses. We examined the relationship of Abs against different viruses to clinical trajectory groups from the National Institutes of Health IMPACC (Immunophenotyping Assessment in a COVID-19 Cohort) study of hospitalized COVID-19 patients. Whereas initial Ab titers to SARS-CoV-2 tended to be higher with increasing severity (excluding fatal disease), those to seasonal coronaviruses trended in the opposite direction. Initial Ab titers to influenza and parainfluenza viruses also tended to be lower with increasing severity. However, no significant relationship was observed for Abs to other viruses, including measles, CMV, EBV, and respiratory syncytial virus. We hypothesize that some individuals may produce lower or less durable Ab responses to respiratory viruses generally (reflected in lower baseline titers in our study), and that this may carry over into poorer outcomes for COVID-19 (despite high initial SARS-CoV-2 titers). We further looked at longitudinal changes in Ab responses to heterologous viruses, but found little change during the course of acute COVID-19 infection. We saw significant trends with age for Ab levels to many of these viruses, but no difference in longitudinal SARS-CoV-2 titers for those with high versus low seasonal coronavirus titers. We detected no difference in longitudinal SARS-CoV-2 titers for CMV seropositive versus seronegative patients, although there was an overrepresentation of CMV seropositives among the IMPACC cohort, compared with expected frequencies in the United States population. Our results both reinforce findings from other studies and suggest (to our knowledge) new relationships between the response to SARS-CoV-2 and Abs to heterologous viruses.

Original languageEnglish
Pages (from-to)1224-1231
Number of pages8
JournalJournal of Immunology
Volume211
Issue number8
DOIs
StatePublished - Oct 15 2023

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