Influence of trem-1 gene polymorphisms on cytokine levels during malaria by Plasmodium vivax in a frontier area of the Brazilian Amazon

•Infected individuals with rs6910730A allele had higher IL-6, IL-10, and IFN-γ levels.•IL-5, IL-6, IL-10, TNF-α, and IFN-γ were increased in rs2234237T and infected.•The rs2234246CT genotype group and infected had higher levels of TNF-α, and IFN-γ.•IFN-γ was higher in the infected group with rs47116...

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Published in:Cytokine (Philadelphia, Pa.) Vol. 169; p. 156264
Main Authors: de Jesus, Myrela C.S., Cerilo-Filho, Marcelo, Ramirez, Aina D.R., Menezes, Rubens A.O., Gomes, Margarete S.M., Cassiano, Gustavo C., Gurgel, Ricardo Q., Silva, José R.S., Moura, Tatiana R., Pratt-Riccio, Lilian R., Baptista, Andrea R.S., Storti-Melo, Luciane M., Machado, Ricardo L.D.
Format: Journal Article
Language:English
Published: England Elsevier Ltd 01-09-2023
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Abstract •Infected individuals with rs6910730A allele had higher IL-6, IL-10, and IFN-γ levels.•IL-5, IL-6, IL-10, TNF-α, and IFN-γ were increased in rs2234237T and infected.•The rs2234246CT genotype group and infected had higher levels of TNF-α, and IFN-γ.•IFN-γ was higher in the infected group with rs4711668C allele.•The trem-1 polymorphisms had no impact of the sTREM-1 levels. The immunopathology during malaria depends on the level of inflammatory response generated. In this scenario, the TREM-1 has been associated with the severity of infectious diseases and could play an important role in the inflammatory course of malaria. We aimed to describe the allelic and genotypic frequency of four polymorphisms in the trem-1 gene in Plasmodium vivax-infected patients and to verify the association of these polymorphisms with clinical and immunological factors in a frontier area of the Brazilian Amazon. We included 76 individuals infected with P. vivax and 144 healthy controls living in the municipality of Oiapoque, Amapá, Brazil. The levels of TNF-α, IL-10, IL-2, IL-4, IL-5, and IFN-γ were measured by flow cytometry, while IL-6, sTREM-1, and antibodies against PvMSP-119 were evaluated by ELISA. The SNPs were genotyped by qPCR technique. Polymorphisms analysis, allelic and genotype, frequencies, and HWE calculation were determined by x2 test in R Software. The association between the parasitemia, gametocytes, antibodies, cytokines, and sTREM-1 with the genotypes of malaria and control groups was performed using the Kruskal-Wallis test, these analyzes were conducted in SPSS Software, at 5% significance level. All SNPs were successfully genotyped. Allelic and genotypic distribution was in Hardy-Weinberg Equilibrium. Furthermore, several associations were identified between malaria and control groups, with increased levels of IL-5, IL-6, IL-10, TNF-α, and IFN-γ in the infected individuals with rs6910730A, rs2234237T, rs2234246T, rs4711668C alleles compared to the homozygous wild-type and heterozygous genotypes of the controls (p-value < 0.05). No association was found for these SNPs and the levels of IL-2, and sTREM-1. The SNPs on the trem-1 gene are associated with the effector molecules of the innate immunity and may contribute to the identification and effective participation of trem-1 in the modulation of the immune response. This association may be essential for the establishment of immunization strategies against malaria.
AbstractList •Infected individuals with rs6910730A allele had higher IL-6, IL-10, and IFN-γ levels.•IL-5, IL-6, IL-10, TNF-α, and IFN-γ were increased in rs2234237T and infected.•The rs2234246CT genotype group and infected had higher levels of TNF-α, and IFN-γ.•IFN-γ was higher in the infected group with rs4711668C allele.•The trem-1 polymorphisms had no impact of the sTREM-1 levels. The immunopathology during malaria depends on the level of inflammatory response generated. In this scenario, the TREM-1 has been associated with the severity of infectious diseases and could play an important role in the inflammatory course of malaria. We aimed to describe the allelic and genotypic frequency of four polymorphisms in the trem-1 gene in Plasmodium vivax-infected patients and to verify the association of these polymorphisms with clinical and immunological factors in a frontier area of the Brazilian Amazon. We included 76 individuals infected with P. vivax and 144 healthy controls living in the municipality of Oiapoque, Amapá, Brazil. The levels of TNF-α, IL-10, IL-2, IL-4, IL-5, and IFN-γ were measured by flow cytometry, while IL-6, sTREM-1, and antibodies against PvMSP-119 were evaluated by ELISA. The SNPs were genotyped by qPCR technique. Polymorphisms analysis, allelic and genotype, frequencies, and HWE calculation were determined by x2 test in R Software. The association between the parasitemia, gametocytes, antibodies, cytokines, and sTREM-1 with the genotypes of malaria and control groups was performed using the Kruskal-Wallis test, these analyzes were conducted in SPSS Software, at 5% significance level. All SNPs were successfully genotyped. Allelic and genotypic distribution was in Hardy-Weinberg Equilibrium. Furthermore, several associations were identified between malaria and control groups, with increased levels of IL-5, IL-6, IL-10, TNF-α, and IFN-γ in the infected individuals with rs6910730A, rs2234237T, rs2234246T, rs4711668C alleles compared to the homozygous wild-type and heterozygous genotypes of the controls (p-value < 0.05). No association was found for these SNPs and the levels of IL-2, and sTREM-1. The SNPs on the trem-1 gene are associated with the effector molecules of the innate immunity and may contribute to the identification and effective participation of trem-1 in the modulation of the immune response. This association may be essential for the establishment of immunization strategies against malaria.
The immunopathology during malaria depends on the level of inflammatory response generated. In this scenario, the TREM-1 has been associated with the severity of infectious diseases and could play an important role in the inflammatory course of malaria. We aimed to describe the allelic and genotypic frequency of four polymorphisms in the trem-1 gene in Plasmodium vivax-infected patients and to verify the association of these polymorphisms with clinical and immunological factors in a frontier area of the Brazilian Amazon. We included 76 individuals infected with P. vivax and 144 healthy controls living in the municipality of Oiapoque, Amapá, Brazil. The levels of TNF-α, IL-10, IL-2, IL-4, IL-5, and IFN-γ were measured by flow cytometry, while IL-6, sTREM-1, and antibodies against PvMSP-1 were evaluated by ELISA. The SNPs were genotyped by qPCR technique. Polymorphisms analysis, allelic and genotype, frequencies, and HWE calculation were determined by x test in R Software. The association between the parasitemia, gametocytes, antibodies, cytokines, and sTREM-1 with the genotypes of malaria and control groups was performed using the Kruskal-Wallis test, these analyzes were conducted in SPSS Software, at 5% significance level. All SNPs were successfully genotyped. Allelic and genotypic distribution was in Hardy-Weinberg Equilibrium. Furthermore, several associations were identified between malaria and control groups, with increased levels of IL-5, IL-6, IL-10, TNF-α, and IFN-γ in the infected individuals with rs6910730A, rs2234237T, rs2234246T, rs4711668C alleles compared to the homozygous wild-type and heterozygous genotypes of the controls (p-value < 0.05). No association was found for these SNPs and the levels of IL-2, and sTREM-1. The SNPs on the trem-1 gene are associated with the effector molecules of the innate immunity and may contribute to the identification and effective participation of trem-1 in the modulation of the immune response. This association may be essential for the establishment of immunization strategies against malaria.
BACKGROUNDThe immunopathology during malaria depends on the level of inflammatory response generated. In this scenario, the TREM-1 has been associated with the severity of infectious diseases and could play an important role in the inflammatory course of malaria. We aimed to describe the allelic and genotypic frequency of four polymorphisms in the trem-1 gene in Plasmodium vivax-infected patients and to verify the association of these polymorphisms with clinical and immunological factors in a frontier area of the Brazilian Amazon. METHODSWe included 76 individuals infected with P. vivax and 144 healthy controls living in the municipality of Oiapoque, Amapá, Brazil. The levels of TNF-α, IL-10, IL-2, IL-4, IL-5, and IFN-γ were measured by flow cytometry, while IL-6, sTREM-1, and antibodies against PvMSP-119 were evaluated by ELISA. The SNPs were genotyped by qPCR technique. Polymorphisms analysis, allelic and genotype, frequencies, and HWE calculation were determined by x2 test in R Software. The association between the parasitemia, gametocytes, antibodies, cytokines, and sTREM-1 with the genotypes of malaria and control groups was performed using the Kruskal-Wallis test, these analyzes were conducted in SPSS Software, at 5% significance level. RESULTSAll SNPs were successfully genotyped. Allelic and genotypic distribution was in Hardy-Weinberg Equilibrium. Furthermore, several associations were identified between malaria and control groups, with increased levels of IL-5, IL-6, IL-10, TNF-α, and IFN-γ in the infected individuals with rs6910730A, rs2234237T, rs2234246T, rs4711668C alleles compared to the homozygous wild-type and heterozygous genotypes of the controls (p-value < 0.05). No association was found for these SNPs and the levels of IL-2, and sTREM-1. CONCLUSIONSThe SNPs on the trem-1 gene are associated with the effector molecules of the innate immunity and may contribute to the identification and effective participation of trem-1 in the modulation of the immune response. This association may be essential for the establishment of immunization strategies against malaria.
ArticleNumber 156264
Author Cassiano, Gustavo C.
Silva, José R.S.
Menezes, Rubens A.O.
Ramirez, Aina D.R.
Moura, Tatiana R.
Pratt-Riccio, Lilian R.
Gurgel, Ricardo Q.
Machado, Ricardo L.D.
Gomes, Margarete S.M.
Cerilo-Filho, Marcelo
Storti-Melo, Luciane M.
Baptista, Andrea R.S.
de Jesus, Myrela C.S.
Author_xml – sequence: 1
  givenname: Myrela C.S.
  surname: de Jesus
  fullname: de Jesus, Myrela C.S.
  email: myrelaj@id.uff.br
  organization: Center for Microorganisms’ Investigation, Department of Microbiology and Parasitology, Biomedical Institute, Fluminense Federal University, Niterói 24020-141, Rio de Janeiro, Brazil
– sequence: 2
  givenname: Marcelo
  surname: Cerilo-Filho
  fullname: Cerilo-Filho, Marcelo
  organization: Center for Microorganisms’ Investigation, Department of Microbiology and Parasitology, Biomedical Institute, Fluminense Federal University, Niterói 24020-141, Rio de Janeiro, Brazil
– sequence: 3
  givenname: Aina D.R.
  surname: Ramirez
  fullname: Ramirez, Aina D.R.
  organization: Center for Microorganisms’ Investigation, Department of Microbiology and Parasitology, Biomedical Institute, Fluminense Federal University, Niterói 24020-141, Rio de Janeiro, Brazil
– sequence: 4
  givenname: Rubens A.O.
  surname: Menezes
  fullname: Menezes, Rubens A.O.
  organization: Postgraduate Program in Applied Microbiology and Parasitology, Biomedical Institute, Fluminense Federal University, Niterói 24210-130, Rio de Janeiro, Brazil
– sequence: 5
  givenname: Margarete S.M.
  surname: Gomes
  fullname: Gomes, Margarete S.M.
  organization: Superintendence of Health Surveillance of the State of Amapá, Macapá 68902-865, Amapá, Brazil
– sequence: 6
  givenname: Gustavo C.
  surname: Cassiano
  fullname: Cassiano, Gustavo C.
  organization: University of Lisbon, 1649-004, Portugal
– sequence: 7
  givenname: Ricardo Q.
  surname: Gurgel
  fullname: Gurgel, Ricardo Q.
  organization: Postgraduate Program in Parasite Biology, Center for Biological and Health Sciences, Federal University of Sergipe, São Cristóvão 49100-000, Sergipe, Brazil
– sequence: 8
  givenname: José R.S.
  surname: Silva
  fullname: Silva, José R.S.
  organization: Postgraduate Program in Parasite Biology, Center for Biological and Health Sciences, Federal University of Sergipe, São Cristóvão 49100-000, Sergipe, Brazil
– sequence: 9
  givenname: Tatiana R.
  surname: Moura
  fullname: Moura, Tatiana R.
  organization: Postgraduate Program in Parasite Biology, Center for Biological and Health Sciences, Federal University of Sergipe, São Cristóvão 49100-000, Sergipe, Brazil
– sequence: 10
  givenname: Lilian R.
  surname: Pratt-Riccio
  fullname: Pratt-Riccio, Lilian R.
  organization: Laboratory for Malaria Research, Oswaldo Cruz Foundation, Oswaldo Cruz Institute, Rio de Janeiro 21040-900, Rio de Janeiro, Brazil
– sequence: 11
  givenname: Andrea R.S.
  surname: Baptista
  fullname: Baptista, Andrea R.S.
  organization: Center for Microorganisms’ Investigation, Department of Microbiology and Parasitology, Biomedical Institute, Fluminense Federal University, Niterói 24020-141, Rio de Janeiro, Brazil
– sequence: 12
  givenname: Luciane M.
  surname: Storti-Melo
  fullname: Storti-Melo, Luciane M.
  organization: Postgraduate Program in Parasite Biology, Center for Biological and Health Sciences, Federal University of Sergipe, São Cristóvão 49100-000, Sergipe, Brazil
– sequence: 13
  givenname: Ricardo L.D.
  surname: Machado
  fullname: Machado, Ricardo L.D.
  organization: Center for Microorganisms’ Investigation, Department of Microbiology and Parasitology, Biomedical Institute, Fluminense Federal University, Niterói 24020-141, Rio de Janeiro, Brazil
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Keywords Plasmodium vivax
TREM-1
Malaria
SNP
trem-1 gene
Language English
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Snippet •Infected individuals with rs6910730A allele had higher IL-6, IL-10, and IFN-γ levels.•IL-5, IL-6, IL-10, TNF-α, and IFN-γ were increased in rs2234237T and...
The immunopathology during malaria depends on the level of inflammatory response generated. In this scenario, the TREM-1 has been associated with the severity...
BACKGROUNDThe immunopathology during malaria depends on the level of inflammatory response generated. In this scenario, the TREM-1 has been associated with the...
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SubjectTerms Malaria
Plasmodium vivax
SNP
TREM-1
trem-1 gene
Title Influence of trem-1 gene polymorphisms on cytokine levels during malaria by Plasmodium vivax in a frontier area of the Brazilian Amazon
URI https://dx.doi.org/10.1016/j.cyto.2023.156264
https://www.ncbi.nlm.nih.gov/pubmed/37327529
https://search.proquest.com/docview/2827253574
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