Cell-Mediated Proteomics, and Serological and Mucosal Humoral Immune Responses after Seasonal Influenza Immunization: Characterization of Serological Responders and Non-Responders

Author:

Carlsson Hanna12ORCID,Brudin Lars234,Serrander Lena56,Hinkula Jorma26ORCID,Tjernberg Ivar12ORCID

Affiliation:

1. Department of Clinical Chemistry and Transfusion Medicine, Region Kalmar County, 39244 Kalmar, Sweden

2. Department of Biomedical and Clinical Sciences, Linköping University, 58183 Linköping, Sweden

3. Department of Clinical Physiology, Region Kalmar County, 39244 Kalmar, Sweden

4. Department of Medicine and Health Sciences, Linköping University, 58183 Linköping, Sweden

5. Department of Clinical Microbiology, Region Östergötland, 58185 Linköping, Sweden

6. Department of Molecular, Infection and Inflammation Centre, Linköping University, 58183 Linköping, Sweden

Abstract

Immunization against influenza through vaccination is the most effective method with which to prevent infection. To assess protection after immunization, analysing humoral response with a hemagglutinin inhibition assay is the gold standard, but cell-mediated immune response has been shown to better correlate with protection in the elderly. Our aim was to explore the influenza-specific cell-mediated and mucosal humoral responses in serologically defined responders and non-responders. We analysed sera for total immunoglobulins (Ig) A, G, and M and nasal swab samples for influenza-specific IgA. Peripheral blood mononuclear cells were stimulated with trivalent influenza vaccine VaxiGripTetra, and supernatants were analysed for influenza-specific responses with the Olink Immune-Oncology panel using a proximity extension assay. We included 73 individuals, of which 69 completed the study with follow-up sampling at one and six months post-vaccination. Of the 73, 51 (70%) were found to be serological responders and 22 (30%) were non-responders. We did not find any significant differences in sex or mucosal humoral response between responders and non-responders; however, a higher IFNγ/IL-10 ratio in individuals ≤65 years of age indicates an enhanced cell-mediated immune response in this age group. Characteristics of the non-responders were found to be higher levels of IgM, Granzyme B and Interleukin 12, and lower levels of C-X-C motif chemokine 13 compared with those of the responders. In conclusion, our results did not show any correlation between serological response and age. Furthermore, the majority of influenza-specific cell-mediated immune markers did not differ between responders and non-responders; the immune marker profile of the non-responders and its contribution to protection is of interest but needs to be further explored.

Funder

Research Council in Southestern Sweden

Publisher

MDPI AG

Reference31 articles.

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