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Highlights • First work using resveratrol as a photosensitizer in antimicrobial photodynamic therapy. • Photoactivated resveratrol has a modified structure to resveratrone and produces singlet oxygen. • Photoactivation of resveatrol in the air pocket model in mice led to an increase in the production of TNF-α and IL-17A, with in vivo bacterial clearance. Abstract Background Among the pathogens, Staphylococcus aureus is the main causative agent of bacterial diseases in the world. In this context, antimicrobial photodynamic therapy (aPDT) appears as a promising tool by means of microbial inactivation with the use of light. aPDT is applied in treatments involving photosensitizers capable of generating oxygen free radicals. Thus, this work proposes the use of resveratrol as a photosensitizer. Methods In vitro tests were performed to determine the antibacterial activity of photoactivated resveratrol with blue LED light, as well as uric acid experiments for verification of singlet oxygen formation. Possible resveratrol structural changes were evaluated by HPLC. In the in vivo assays, the air pouch model was performed in mice for antimicrobial activity and cytokine production. Results The photoactivated resveratrol exhibited an increase in its antibacterial action and it is possibly brought about by the singlet oxygen formation. In the air pouch model, TNF-α and IL-17A cytokines were produced, diminishing the bacterial load, and consequently, reducing inflammation after 24 h of infection. Cellular number decrease in the inflammatory environment was associated with resolution of inflammation along with greater IL-10 production. Conclusion It is the first time that resveratrol has been associated with aPDT. It was demonstrated in this work that resveratrol activated by blue LED light can be a promising photosensitizer. This compound, after the light stimulus, produces singlet oxygen, in addition to having effects on the immune system triggering TNF-α and IL-17A production, aiding in the clearance of several bacteria, including S. aureus. [ABSTRACT FROM AUTHOR]

Coinfection with leishmaniasis and schistosomiasis has been associated with increased time to healing of cutaneous lesions of leishmaniasis. The objective of this study was to evaluate the effect of Leishmania braziliensis infection on co-cultures of monocyte-derived dendritic cells (MoDCs) with autologous lymphocytes from patients with schistosomiasis and patients with cutaneous leishmaniasis. MoDCs were differentiated from peripheral blood monocytes, isolated by magnetic beads, infected with L. braziliensis , and co-cultured with autologous lymphocytes. Expression of HLA-DR, CD1a, CD83, CD80, CD86, CD40, and the IL-10 receptor (IL-10R) on MoDCs as well as CD28, CD40L, CD25, and CTLA-4 on lymphocytes were evaluated by flow cytometry. The production of the cytokines IL-10, TNF, IL-12p40, and IFN-γ were evaluated by sandwich ELISA of the culture supernatant. The infectivity evaluation was performed by light microscopy after concentration of cells by cytospin and Giemsa staining. It was observed that the frequency of MoDCs expressing CD83, CD80, and CD86 as well as the MFI of HLA-DR were smaller in the group of patients with schistosomiasis compared to the group of patients with leishmaniasis. On the other hand, the frequency of IL-10R on MoDCs was higher in patients with schistosomiasis than in patients with leishmaniasis. CD4 + and CD8 + T lymphocytes from patients with schistosomiasis presented a lower frequency of CD28 and a higher frequency of CTLA-4 compared to lymphocytes from patients with leishmaniasis. Levels of IL-10 were higher in the supernatants of co-cultures from individuals with schistosomiasis compared to those with leishmaniasis. However, levels of TNF, IL-12p40, and IFN-γ were lower in the group of individuals with schistosomiasis. Regarding the frequency of MoDCs infected by L. braziliensis after 72 h in culture, it was observed that higher frequencies of cells from patients with schistosomiasis were infected compared to cells from patients with leishmaniasis. It was concluded that MoDCs from patients with schistosomiasis are more likely to be infected by L. braziliensis , possibly due to a lower degree of activation and a regulatory profile. [ABSTRACT FROM AUTHOR]

Aging in women is characterized by extreme hormonal changes leading them to develop a chronic low-grade inflammation that is linked to the development of systemic arterial hypertension (SAH) and type 2 diabetes mellitus (T2DM). In this scenario, physical activity emerges as an interesting methodology, since it seems to be connected to a decrease in serum levels of some pro-inflammatory cytokines. Nevertheless, most studies evaluate these cytokines in an isolated manner not considering the influence of comorbidities on the responsiveness of participants to the benefits of physical activity. So, this study aimed to assess the influence of physical activity on body composition, anthropometric parameters, lipid profile, and inflammatory markers of diabetic and hypertensive older postmenopausal women. We evaluated 163 women aged from 60 to 80 years, diagnosed with T2DM and SAH that were assisted by the Family Health Units in Vitória da Conquista, Bahia, Brazil. The pratice of physical activity was measured by the International Physical Activity Questionnaire with the participants being classified as active or sedentary individuals. Active older women presented better body composition, lipid profile and inflammatory balance. This was connected to a better correlation profile between these factors in active older women, characteristics that were not noticed in sedentary older women. Moreover, IL-17A and the relationship between IL-10 and the other pro-inflammatory cytokines examined was greatly influenced by physical activity. Consequently, physical activity is linked to a global improvement in T2DM and SAH risk factors and with a positive inflammatory modulation in diabetic and hypertensive older women. • Physical activity reduces inflammaging in older women with diabetes and hypertension; • Physical activity interferes with the correlation pattern of inflammatory markers; • Active older women have a better balance between IL-10 and IL-17. [ABSTRACT FROM AUTHOR]

Asthma is a chronic disease characterized by airway inflammation, obstruction and hyperresponsiveness. Severe asthma affects a small proportion of subjects but results in most of the morbidity, costs and mortality associated with the disease. Studies have suggested that Schistosoma mansoni infection reduces the severity of asthma and prevent atopy. Objective We evaluated the ability of S. mansoni antigens, Sm29 and Sm29TSP-2 to modulate lymphocyte activation status in response to the allergen of the mite Dermatophagoides pteronyssinus ( Der p 1) in cell cultures of individuals with asthma. Methods Thirty four patients were enrolled in this study: seventeen patients with severe asthma (SA group), seventeen patients with mild asthma (MA group) and six controls with no asthma. Peripheral blood mononuclear cells (PBMC) were obtained and stimulated with Sm29 and Sm29TSP-2 in the presence or absence of Der p1 . The expression of surface markers and cytokines on lymphocytes was evaluated by flow cytometry and the levels of IL-10 in the culture supernatant were determined by ELISA. Results The addition of Sm29 and Sm29TSP-2 antigens to PBMC cultures from both groups of subjects with asthma stimulated with Der p 1 reduced the frequency of CD4 + CD25 low cells whereas and increased frequency of CD4 + CD25 high population was observed compared to unstimulated cultures. Moreover, cultures stimulated with Sm29TSP-2 showed a reduction in the frequency of T cells expressing CD69, IFN-γ, TNF and TGF-β in the MA group and an increase in the frequency of CD4 + TSLPR + T cells in the SA group. The addition of Sm29 to the cultures reduced the frequency of CD4 + CD69 + and CD4 + IL-5 + T cells in all asthmatic groups, and reduced the frequency of CD4 + T cells expressing IL-13 in the MA group. The cultures stimulated with Sm29 and Sm29TSP-2 showed an increase in the level of IL-10 in the supernatants. Conclusion These results suggest that the addition of Sm29 and Sm29TSP-2 to the cells cultures from subjects with asthma reduced cell activation markers and altered the cytokine production pattern in a way that can potentialy control the inflammatory response associated with asthma. [ABSTRACT FROM AUTHOR]