tetano
Editor, Senior Moderator
Am J Transplant
. 2021 Jan 23.
doi: 10.1111/ajt.16503. Online ahead of print.
Natural Influenza Infection produces a greater Diversity of Humoral Responses than Vaccination in Immunosuppressed Transplant Recipients
Cedric Hirzel[SUP] 1 2 [/SUP], Andrzej Chruscinski[SUP] 3 [/SUP], Victor H Ferreira[SUP] 1 [/SUP], Arnaud G L'Huillier[SUP] 4 [/SUP], Yochiro Natori[SUP] 5 [/SUP], Sang Hoon Han[SUP] 6 [/SUP], Elisa Cordero[SUP] 7 8 [/SUP], Atul Humar[SUP] 1 [/SUP], Deepali Kumar[SUP] 1 [/SUP], Influenza In Transplant Study Group
Affiliations
Abstract
The humoral immune response to influenza virus infection is complex and may be different compared to the antibody response elicited by vaccination. We analyzed the breadth of IgG and IgA responses in solid organ transplant recipients to a diverse collection of 86 influenza antigens elicited by natural influenza A virus (IAV) infection or by vaccination. Antibody levels were quantified using a custom antigen microarray. A total of 120 patients were included: 80 IAV infected (40 A/H1N1, 40 A/H3N2) and 40 vaccinated. Based on hierarchical clustering analysis, infection with either H1N1 or H3N2 virus showed a more diverse antibody response compared to vaccination. Similarly, H1N1 infected individuals showed a significant IgG response to 27.9% of array antigens, H3N2 infected patients to 43.0% of antigens, whereas vaccination elicited a less broad immune response (7.0% of antigens). Immune responses were not exclusively targeting influenza hemagglutinin proteins but were also directed against conserved influenza antigens. Serum IgA responses followed a similar profile. This study provides novel data on the breadth of antibody responses to influenza. We also found that the diversity of response is greater in influenza infected rather than vaccinated patients, providing a potential mechanistic rationale for suboptimal vaccine efficacy in this population.
. 2021 Jan 23.
doi: 10.1111/ajt.16503. Online ahead of print.
Natural Influenza Infection produces a greater Diversity of Humoral Responses than Vaccination in Immunosuppressed Transplant Recipients
Cedric Hirzel[SUP] 1 2 [/SUP], Andrzej Chruscinski[SUP] 3 [/SUP], Victor H Ferreira[SUP] 1 [/SUP], Arnaud G L'Huillier[SUP] 4 [/SUP], Yochiro Natori[SUP] 5 [/SUP], Sang Hoon Han[SUP] 6 [/SUP], Elisa Cordero[SUP] 7 8 [/SUP], Atul Humar[SUP] 1 [/SUP], Deepali Kumar[SUP] 1 [/SUP], Influenza In Transplant Study Group
Affiliations
- PMID: 33484237
- DOI: 10.1111/ajt.16503
Abstract
The humoral immune response to influenza virus infection is complex and may be different compared to the antibody response elicited by vaccination. We analyzed the breadth of IgG and IgA responses in solid organ transplant recipients to a diverse collection of 86 influenza antigens elicited by natural influenza A virus (IAV) infection or by vaccination. Antibody levels were quantified using a custom antigen microarray. A total of 120 patients were included: 80 IAV infected (40 A/H1N1, 40 A/H3N2) and 40 vaccinated. Based on hierarchical clustering analysis, infection with either H1N1 or H3N2 virus showed a more diverse antibody response compared to vaccination. Similarly, H1N1 infected individuals showed a significant IgG response to 27.9% of array antigens, H3N2 infected patients to 43.0% of antigens, whereas vaccination elicited a less broad immune response (7.0% of antigens). Immune responses were not exclusively targeting influenza hemagglutinin proteins but were also directed against conserved influenza antigens. Serum IgA responses followed a similar profile. This study provides novel data on the breadth of antibody responses to influenza. We also found that the diversity of response is greater in influenza infected rather than vaccinated patients, providing a potential mechanistic rationale for suboptimal vaccine efficacy in this population.