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).
COVID-19 vaccines
SARS-COV-2 antibody
SARS-CoV-2 neutralization
immunocompromised
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
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-e644Subventions
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.
Références
Cancer Cell. 2021 Aug 9;39(8):1091-1098.e2
pubmed: 34214473
NPJ Vaccines. 2022 Jan 27;7(1):14
pubmed: 35087066
N Engl J Med. 2020 Nov 12;383(20):1920-1931
pubmed: 32663912
J Infect Dis. 2017 Dec 19;216(12):1525-1533
pubmed: 29253205
JAMA Oncol. 2021 Aug 1;7(8):1133-1140
pubmed: 34047765
JAMA. 2021 Oct 19;326(15):1533-1535
pubmed: 34459863
Nature. 2020 Oct;586(7830):589-593
pubmed: 32785213
N Engl J Med. 2021 Feb 4;384(5):403-416
pubmed: 33378609
Eur J Heart Fail. 2021 Sep;23(9):1555-1559
pubmed: 33963635
Blood Adv. 2021 Jun 21;5(12):2624-2643
pubmed: 34152403
Am J Transplant. 2021 Aug;21(8):2719-2726
pubmed: 33866672
Ann Intern Med. 2021 Sep;174(9):1330-1332
pubmed: 34125572
J Hepatol. 2021 Aug;75(2):435-438
pubmed: 33892006
N Engl J Med. 2020 Dec 31;383(27):2603-2615
pubmed: 33301246
J Biomed Inform. 2009 Apr;42(2):377-81
pubmed: 18929686
JAMA. 2020 Jan 7;323(1):19-20
pubmed: 31825458
Am J Clin Oncol. 2018 Mar;41(3):248-253
pubmed: 26669741
N Engl J Med. 2021 Aug 12;385(7):661-662
pubmed: 34161700
N Engl J Med. 2021 Sep 23;385(13):1244-1246
pubmed: 34379917
Am J Clin Pathol. 2021 Feb 11;155(3):343-353
pubmed: 33155015
J Appl Lab Med. 2021 Mar 1;6(2):486-490
pubmed: 33367709
MMWR Morb Mortal Wkly Rep. 2021 Sep 24;70(38):1337-1343
pubmed: 34555004
N Engl J Med. 2021 Aug 12;385(7):585-594
pubmed: 34289274
J Am Med Dir Assoc. 2021 Aug;22(8):1593-1598
pubmed: 34129831
JAMA. 2021 Jun 1;325(21):2204-2206
pubmed: 33950155
Cancer Cell. 2021 Aug 9;39(8):1081-1090.e2
pubmed: 34133951