Prospective Evaluation of Coronavirus Disease 2019 (COVID-19) Vaccine Responses Across a Broad Spectrum of Immunocompromising Conditions: the COVID-19 Vaccination in the Immunocompromised Study (COVICS).


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
24 08 2022
Historique:
received: 31 10 2021
pubmed: 19 2 2022
medline: 30 8 2022
entrez: 18 2 2022
Statut: ppublish

Résumé

We studied humoral responses after coronavirus disease 2019 (COVID-19) vaccination across varying causes of immunodeficiency. Prospective study of fully vaccinated immunocompromised adults (solid organ transplant [SOT], hematologic malignancy, solid cancers, autoimmune conditions, human immunodeficiency virus [HIV]) versus nonimmunocompromised healthcare workers (HCWs). The primary outcome was the proportion with a reactive test (seropositive) for immunoglobulin G to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) receptor-binding domain. Secondary outcomes were comparisons of antibody levels and their correlation with pseudovirus neutralization titers. Stepwise logistic regression was used to identify factors associated with seropositivity. A total of 1271 participants enrolled: 1099 immunocompromised and 172 HCW. Compared with HCW (92.4% seropositive), seropositivity was lower among participants with SOT (30.7%), hematological malignancies (50.0%), autoimmune conditions (79.1%), solid tumors (78.7%), and HIV (79.8%) (P < .01). Factors associated with poor seropositivity included age, greater immunosuppression, time since vaccination, anti-CD20 monoclonal antibodies, and vaccination with BNT162b2 (Pfizer) or adenovirus vector vaccines versus messenger RNA (mRNA)-1273 (Moderna). mRNA-1273 was associated with higher antibody levels than BNT162b2 or adenovirus vector vaccines after adjusting for time since vaccination, age, and underlying condition. Antibody levels were strongly correlated with pseudovirus neutralization titers (Spearman r = 0.89, P < .0001), but in seropositive participants with intermediate antibody levels, neutralization titers were significantly lower in immunocompromised individuals versus HCW. Antibody responses to COVID-19 vaccines were lowest among SOT and anti-CD20 monoclonal recipients, and recipients of vaccines other than mRNA-1273. Among those with intermediate antibody levels, pseudovirus neutralization titers were lower in immunocompromised patients than HCWs. Additional SARS-CoV-2 preventive approaches are needed for immunocompromised persons, which may need to be tailored to the cause of immunodeficiency.

Sections du résumé

BACKGROUND
We studied humoral responses after coronavirus disease 2019 (COVID-19) vaccination across varying causes of immunodeficiency.
METHODS
Prospective study of fully vaccinated immunocompromised adults (solid organ transplant [SOT], hematologic malignancy, solid cancers, autoimmune conditions, human immunodeficiency virus [HIV]) versus nonimmunocompromised healthcare workers (HCWs). The primary outcome was the proportion with a reactive test (seropositive) for immunoglobulin G to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) receptor-binding domain. Secondary outcomes were comparisons of antibody levels and their correlation with pseudovirus neutralization titers. Stepwise logistic regression was used to identify factors associated with seropositivity.
RESULTS
A total of 1271 participants enrolled: 1099 immunocompromised and 172 HCW. Compared with HCW (92.4% seropositive), seropositivity was lower among participants with SOT (30.7%), hematological malignancies (50.0%), autoimmune conditions (79.1%), solid tumors (78.7%), and HIV (79.8%) (P < .01). Factors associated with poor seropositivity included age, greater immunosuppression, time since vaccination, anti-CD20 monoclonal antibodies, and vaccination with BNT162b2 (Pfizer) or adenovirus vector vaccines versus messenger RNA (mRNA)-1273 (Moderna). mRNA-1273 was associated with higher antibody levels than BNT162b2 or adenovirus vector vaccines after adjusting for time since vaccination, age, and underlying condition. Antibody levels were strongly correlated with pseudovirus neutralization titers (Spearman r = 0.89, P < .0001), but in seropositive participants with intermediate antibody levels, neutralization titers were significantly lower in immunocompromised individuals versus HCW.
CONCLUSIONS
Antibody responses to COVID-19 vaccines were lowest among SOT and anti-CD20 monoclonal recipients, and recipients of vaccines other than mRNA-1273. Among those with intermediate antibody levels, pseudovirus neutralization titers were lower in immunocompromised patients than HCWs. Additional SARS-CoV-2 preventive approaches are needed for immunocompromised persons, which may need to be tailored to the cause of immunodeficiency.

Identifiants

pubmed: 35179197
pii: 6530582
doi: 10.1093/cid/ciac103
pmc: PMC8903515
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0
BNT162 Vaccine N38TVC63NU

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e630-e644

Subventions

Organisme : NIAID NIH HHS
ID : K23 AI154546
Pays : United States

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

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Auteurs

Ghady Haidar (G)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Mounzer Agha (M)

Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Andrew Bilderback (A)

Wolff Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Amy Lukanski (A)

Wolff Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Kelsey Linstrum (K)

Health Care Innovation, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Rachel Troyan (R)

Wolff Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Scott Rothenberger (S)

Division of General Internal Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Deborah K McMahon (DK)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Melissa D Crandall (MD)

Clinical Laboratory, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Michele D Sobolewksi (MD)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

P Nathan Enick (P)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Jana L Jacobs (JL)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Kevin Collins (K)

Clinical Analytics, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Cynthia Klamar-Blain (C)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Bernard J C Macatangay (BJC)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Urvi M Parikh (UM)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Amy Heaps (A)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Lindsay Coughenour (L)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Marc B Schwartz (MB)

Division of Gastroenterology, Hepatology and Nutrition, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Jeffrey M Dueker (JM)

Division of Gastroenterology, Hepatology and Nutrition, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Fernanda P Silveira (FP)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Mary E Keebler (ME)

Department of Cardiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Abhinav Humar (A)

Division of Transplantation, Department of Surgery, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

James D Luketich (JD)

Department of Cardiothoracic Surgery, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Matthew R Morrell (MR)

Division of Pulmonary and Critical Care, School of Medicine, University of Utah, Salt Lake City, Utah, USA.

Joseph M Pilewski (JM)

Division of Pulmonary, Allergy and Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

John F McDyer (JF)

Division of Pulmonary, Allergy and Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Bhanu Pappu (B)

Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Robert L Ferris (RL)

Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Stanley M Marks (SM)

Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

John Mahon (J)

Clinical Laboratory, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Katie Mulvey (K)

Clinical Laboratory, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Sundaram Hariharan (S)

Division of Transplantation, Department of Surgery, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Transplant Nephrology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Glenn M Updike (GM)

Department of Obstetrics, Gynecology & Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania, USAand.

Lorraine Brock (L)

Wolff Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Robert Edwards (R)

Department of Obstetrics, Gynecology & Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania, USAand.

Richard H Beigi (RH)

Department of Obstetrics, Gynecology & Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania, USAand.

Paula L Kip (PL)

Wolff Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Alan Wells (A)

Clinical Laboratory, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Tami Minnier (T)

Wolff Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Derek C Angus (DC)

Health Care Innovation, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

John W Mellors (JW)

Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

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