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Porcine reproductive and respiratory syndrome virus (PRRSV) and Streptococcus suis antigens represent a combination of immunogenic components derived from two of the most significant pathogens in the global swine industry [1, 2]. PRRSV is a positive-sense RNA virus that primarily infects porcine alveolar macrophages, leading to severe reproductive failure in sows and respiratory distress in growing pigs [1]. Streptococcus suis is a Gram-positive bacterium that often acts as a secondary opportunistic pathogen following PRRSV-induced immunosuppression, causing systemic diseases such as meningitis, arthritis, and septicemia [2, 3]. Together, these pathogens are major contributors to the Porcine Respiratory Disease Complex (PRDC), resulting in substantial economic losses [3]. Therapeutic strategies focusing on these antigens primarily involve the development of vaccines designed to elicit robust humoral and cellular immune responses [4]. PRRSV antigens typically include the nucleocapsid (N) and envelope proteins (GP5), while S. suis antigens often involve the capsular polysaccharide or various surface proteins [1, 2]. A major challenge in targeting these antigens is the high genetic variability of PRRSV and the numerous serotypes of S. suis, which complicate the achievement of broad cross-protection [1, 2]. Effective management requires multi-valent or broad-spectrum vaccine approaches to address the diversity of circulating strains [4, 5].
Induction of active immunity through the presentation of viral and bacterial epitopes to the host immune system, leading to the production of neutralizing antibodies and activation of cell-mediated immunity (T-cell response) to prevent or mitigate infection [4].
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