Innate immune cells show enhanced responsiveness to secondary challenges after an initial non-related stimulation (Trained Innate Immunity, TII). Acute NOD2 activation by Muramyl-Dipeptide (MDP) promotes TII inducing the secretion of pro-inflammatory mediators, while a sustained MDP-stimulation down-regulates the inflammatory response, restoring tolerance. Here we characterized in-vitro the response of murine macrophages to lipopolysaccharide (LPS) challenge under NOD2-chronic stimulation. RAW264.7 cells were trained with MDP (1 mu g/ml, 48 h) and challenged with LPS (5 mu g/ml, 24 h). Trained cells formed multinucleated giant cells with increased phagocytosis rates compared to untrained/challenged cells. They showed a reduced mitochondrial activity and a switch to aerobic glycolysis. TNF-alpha, ROS and NO were upregulated in both trained and untrained cultures (MDP+, MDP- cells, p > 0.05); while IL-10, IL-6 IL-12 and MHCII were upregulated only in trained cells after LPS challenge (MDP + LPS+, p < 0.05). A slight upregulation in the expression of B7.2 was also observed in this group, although differences were not statistically significant. MDP-training induced resistance to LPS challenge (p < 0.01). The relative expression of PARP-1 was downregulated after the LPS challenge, which may contribute to the regulatory milieu and to the innate memory mechanisms exhibited by MDP-trained cells. Our results demonstrate that a sustained MDP-training polarizes murine macrophages towards a M2b profile, inhibiting parthanatos. These results may impact on the development of strategies to immunomodulate processes in which inflammation should be controlled.

El objetivo de este trabajo fue conocer la seroprevalencia de Neospora caninum en los bovinos de los tambos del Valle del Lerma (Salta, Argentina) y los factores de riesgo asociados a la transmisión de este parásito en esta región. Se tomaron muestras de suero de aproximadamente 40 vacas en cada tambo, que fueron analizadas por ELISA indirecto para detectar anticuerpos contra N. caninum. También se discriminó entre infecciones crónicas y agudas midiendo la avidez de dichos anticuerpos. Todos los tambos presentaron al menos un bovino seropositivo y la media fue de 35,3 ± 14,9% de animales positivos. También se detectaron anticuerpos específicos en caninos presentes en 9 de los 16 tambos, con un valor de seropositividad del 71,7 ± 19,9%. El 56,3% de los bovinos seropositivos cursaban infecciones agudas. Se halló una asociación negativa entre la seroprevalencia y el índice de avidez de los anticuerpos específicos, lo que indica que la presencia de animales con infecciones agudas se asocia a mayor seroprevalencia. Los campos con pastoreo presentaron mayor cantidad de infecciones recientes. Estos resultados revelan por primera vez la importancia de este parásito en los tambos de la región y la necesidad de propiciar el desarrollo de programas de control considerando los distintos factores de riesgo que afectan la situación epidemiológica de la enfermedad. The objective of this work was to determine the seroprevalence of Neospora caninum in cattle in Valle de Lerma, province of Salta, Argentina, and the risk factors associated with the disease. Serum samples were taken from 40 cows in each dairy herd, which were analyzed by indirect ELISA to detect antibodies against N. caninum. Chronic and acute infections were discriminated by measuring the avidity of these antibodies. All the herds exhibited at least one seropositive animal, the mean being 35.3 ± 14.9% of positive animals. Specific antibodies were also detected in dogs present in 9 of the herds, which showed a seropositivity value of 71.7% ± 19.9%. Among the seropositive animals, 56.3% showed acute infections. A negative association was found between seroprevalence and the avidity index of specific antibodies, indicating that the presence of animals with acute infections is associated with higher seroprevalence. Fields with grazing showed more recent infections. These results show for the first time the importance of this parasite in this particular region and the need to promote the development of control programs considering the different risk factors that affect the epidemiological situation of the disease.

Background/Objectives: Vaccine immunogenicity is often suboptimal in vulnerable populations such as the elderly, infants, and individuals in low- and middle-income countries. One contributing factor may be pre-existing immunomodulatory conditions, including helminth infections. This study investigates the impact of Fasciola hepatica (F. hepatica) derived molecules on the early humoral response to the COVID-19 mRNA vaccine Comirnaty^® in a mouse model. Methods: BALB/c mice were pretreated with a F. hepatica protein extract (FH) or complete Freund’s adjuvant (CFA) prior to vaccination. Cytokine production and antibody responses were assessed at 0, 14, and 21 days post-vaccination (dpv) through serum analysis and ex vivo splenocyte stimulation with the SARS-CoV-2 receptor-binding domain (RBD) or LPS. Results: At 0 dpv, FH-treated mice showed increased serum IL-10, while CFA treatment induced IL-12. FH- but not CFA-treated splenocytes secreted IL-10 upon RBD or LPS stimulation. At 21 dpv, FH-treated mice lacked IFN-γ production but maintained IL-10 and showed elevated IL-4, consistent with a Th2-skewed profile. Although total anti-RBD IgG levels were similar between groups, FH-treated mice exhibited reduced IgG avidity and a higher IgG1/IgG2 ratio. CFA-treated mice showed delayed avidity maturation. Conclusions: Prior exposure to F. hepatica antigens can modulate the early immune response to Comirnaty^®, affecting both cellular activation and antibody quality. This altered response may reflect a reduced early protective capacity of the vaccine, which might need to be considered when designing or evaluating vaccination strategies using mRNA vaccines in helminth-endemic regions.

Objetive. Conventional control measures for rhinotracheitis caused by bovine alphaherpesvirus 1 (BoAHV-1, IBR) include vaccination and hygienic measures for herd cattle. In this study, an antiparasitic (Ivermectin) drug was evaluated for the potential treatment of BoAHV-1 in bovines. Materials and Methods. Fifteen bovines were randomly assigned to three groups (n=5 per group). Group 1 received no treatment. Group 2 was subcutaneously vaccinated with 3 mL of a commercial inactivated BoAHV-1 vaccine (Biopoligen Air) 30 and 9 days prior to viral challenge. Group 3 was treated with ivermectin (IVOMEC 1%, 0.2 mg/kg) at 0 and 5 days post-challenge. All animals were challenged intranasal with 3 mL of virulent BoAHV-1 (107.5 TCID₅₀/mL). Clinical signs were scored daily for 22 days post-challenge (dpc), and nasal secretions were collected for 14 dpc to assess viral shedding. Results. The efficacy of Ivermectin in inhibiting BoAHV-1 replication during peak infection days was notable, demonstrating a reduction of 1.5-2.25 logs compared to the infection control group. This inhibition was significant on day 6, coinciding with the peak excretion observed in the infection control group. Although replication was significantly reduced in animals challenged and treated with IVM, a question that was not answered is whether this replication was sufficient to establish latency. Therefore, it remains pending for future investigations to immunosuppress and evaluate the reactivation of latency. Conclusions. The findings of this study demonstrate that Ivermectin administered at the beginning of the infection and with reinforcement at 5 days was effective in reducing clinical signs of disease and viral excretion following the BoAHV-1 challenge. These findings demonstrate the inhibitory effect of ivermectin on BoAHV-1 replication in vivo and offer an alternative complementary strategy for managing and controlling BoAHV-1 outbreaks.