TY - JOUR
T1 - Biological and inflammatory effects of antigen 5 from polybia paulista (Hymenoptera, vespidae) venom in mouse intraperitoneal macrophages
AU - Bazon, Murilo Luiz
AU - Fernandes, Luis Gustavo Romani
AU - Assugeni, Isabela Oliveira Sandrini
AU - Pinto, Lucas Machado
AU - Simioni, Patrícia Ucelli
AU - de Lima Zollner, Ricardo
AU - Braga, Márcia Regina Brochetto
N1 - Funding Information:
Funding: This research was funded by São Paulo Research Foundation (FAPESP) (Grant No. 2017/07988-2 and no 2019/02298-3 to M.L.B. and Grant nº. 2017/18422-0 to M.R.B.B.).
Funding Information:
Acknowledgments: We acknowledge the financial support from São Paulo Research Foundation (FAPESP) (Grant no. 2017/07988-2 and no. 2019/02298-3 to M.L.B. and Grant No. 2017/18422-0 to M.R.B.B.). The authors also thank Postgraduate Program of Biological Sciences (Cellular and Molecular Biology) at State University of São Paulo (UNESP), Rio Claro.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/12
Y1 - 2021/12
N2 - The social wasp Polybia paulista (Hymenoptera, Vespidae) is highly aggressive, being responsible for many medical occurrences. One of the most allergenic components of this venom is Antigen 5 (Poly p 5). The possible modulation of the in vitro immune response induced by antigen 5 from P. paulista venom, expressed recombinantly (rPoly p 5), on BALB/c mice peritoneal macrophages, activated or not with LPS, was assessed. Here, we analyzed cell viability changes, expression of the phosphorylated form of p65 NF-κB subunit, nitric oxide (NO), proinflammatory cytokines production, and co-stimulatory molecules (CD80, CD86). The results suggest that rPoly p 5 does not affect NO production nor the expression of co-stimulatory molecules in mouse peritoneal macrophages. On the other hand, rPoly p 5 induced an increase in IL-1β production in non-activated macrophages and a reduction in the production of TNF-α and MCP-1 cytokines in activated macrophages. rPoly p 5 decreased the in vitro production of the phosphorylated p65 NF-κB subunit in non-activated macrophages. These findings suggest an essential role of this allergen in the polarization of functional M2 macrophage phenotypes, when analyzed in previously activated macrophages. Further investigations, mainly in in vivo studies, should be conducted to elucidate Polybia paulista Ag5 biological role in the macrophage functional profile modulation.
AB - The social wasp Polybia paulista (Hymenoptera, Vespidae) is highly aggressive, being responsible for many medical occurrences. One of the most allergenic components of this venom is Antigen 5 (Poly p 5). The possible modulation of the in vitro immune response induced by antigen 5 from P. paulista venom, expressed recombinantly (rPoly p 5), on BALB/c mice peritoneal macrophages, activated or not with LPS, was assessed. Here, we analyzed cell viability changes, expression of the phosphorylated form of p65 NF-κB subunit, nitric oxide (NO), proinflammatory cytokines production, and co-stimulatory molecules (CD80, CD86). The results suggest that rPoly p 5 does not affect NO production nor the expression of co-stimulatory molecules in mouse peritoneal macrophages. On the other hand, rPoly p 5 induced an increase in IL-1β production in non-activated macrophages and a reduction in the production of TNF-α and MCP-1 cytokines in activated macrophages. rPoly p 5 decreased the in vitro production of the phosphorylated p65 NF-κB subunit in non-activated macrophages. These findings suggest an essential role of this allergen in the polarization of functional M2 macrophage phenotypes, when analyzed in previously activated macrophages. Further investigations, mainly in in vivo studies, should be conducted to elucidate Polybia paulista Ag5 biological role in the macrophage functional profile modulation.
KW - Antigen 5
KW - Hymenoptera
KW - Inflammatory effects
KW - Macrophages
KW - Polybia paulista
UR - http://www.scopus.com/inward/record.url?scp=85120798406&partnerID=8YFLogxK
UR - https://pubmed.ncbi.nlm.nih.gov/34941688
U2 - 10.3390/toxins13120850
DO - 10.3390/toxins13120850
M3 - Article
C2 - 34941688
AN - SCOPUS:85120798406
SN - 2072-6651
VL - 13
JO - Toxins
JF - Toxins
IS - 12
M1 - 850
ER -