Su J, Hamway Y, Mistretta D, Liao BH, Ma Z, Schluckebier J, Xie Z, Polezhaeva O, Jradi W, Braun S, Robb J, Main LF, Mukherjee P, Jubran-Rudolf L, Steiger K, Pino P, Tenbusch M, D'Ippolito E, Ebert G, Protzer U, Prazeres da Costa C (2026)
Publication Type: Journal article
Publication year: 2026
Book Volume: 17
Pages Range: 1827532-
DOI: 10.3389/fimmu.2026.1827532
Objectives: Helminth parasites infect over a quarter of the global population and can profoundly modulate host immunity, potentially influencing vaccine performance and the spread of pandemic pathogens such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Despite the high global endemicity of helminth infections, their impact on immune responses to various COVID-19 vaccines remains unknown. This study aimed to evaluate the impact of Schistosoma infection on the immunogenicity and protective efficacy of messenger RNA (mRNA)- and protein-based COVID-19 vaccines. Methods: Mice with Schistosoma infection and non-infected controls were immunized with either an mRNA-based COVID-19 vaccine or an alum-adjuvanted spike protein vaccine. Vaccine-induced humoral and cellular immune responses were assessed, and protective efficacy was evaluated using a SARS-CoV-2 challenge model. Results: COVID-19 mRNA vaccination induced strong spike-specific antibody and CD4 T-cell responses in Schistosoma-infected mice comparable to non-infected controls, despite a Th2/regulatory-biased immune environment, although multifunctional CD8 T-cell responses were reduced. Alum-adjuvanted protein vaccination elicited robust humoral but weaker cellular immunity, with comparable immune responses in infected and non-infected mice. Following SARS-CoV-2 challenge, both vaccine platforms conferred effective protection, with substantial viral clearance and minimal lung pathology. Conclusions: mRNA and protein vaccines elicit distinct immune profiles; however, both protect effectively against SARS-CoV-2 infection in mice with concurrent helminth infection.
APA:
Su, J., Hamway, Y., Mistretta, D., Liao, B.H., Ma, Z., Schluckebier, J.,... Prazeres da Costa, C. (2026). Helminth infection modulates the immunogenicity of COVID-19 vaccines in mice without compromising protective efficacy. Frontiers in Immunology, 17, 1827532-. https://doi.org/10.3389/fimmu.2026.1827532
MLA:
Su, Jinpeng, et al. "Helminth infection modulates the immunogenicity of COVID-19 vaccines in mice without compromising protective efficacy." Frontiers in Immunology 17 (2026): 1827532-.
BibTeX: Download