IgG subclasses pattern and high-avidity antibody to the C-terminal region of merozoite surface protein 1 of Plasmodium vivax in an unstable hypoendemic region in Iran
The C-terminal region of Plasmodium vivax merozoite surface protein 1 (PvMSP-1 19) is a leading vaccine candidate for inclusion in a polyvalent malaria vaccine. In the present study, the IgG subclasses profile and the avidity of IgG to PvMSP-1 19 were evaluated in individuals ( n = 94) naturally exp...
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Published in | Acta tropica Vol. 112; no. 1; pp. 1 - 7 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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01.10.2009
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Abstract | The C-terminal region of
Plasmodium vivax merozoite surface protein 1 (PvMSP-1
19) is a leading vaccine candidate for inclusion in a polyvalent malaria vaccine. In the present study, the IgG subclasses profile and the avidity of IgG to PvMSP-1
19 were evaluated in individuals (
n
=
94) naturally exposed to
P. vivax parasite in malaria endemic areas in Chabahar districts, Iran. In individuals with patent
P. vivax malaria, 86.1% was sero-positive to PvMSP-1
19 and IgG1 (81.9%) was the predominant subclass. In addition, to determine the persistence of specific IgG, IgG1 and IgG3 antibodies to PvMSP-1
19, the frequency of antibodies was determined in the infected subjects (
n
=
74) after treatment with standard chloroquine and it was detected that the frequency of responders was significantly reduced to 51.3%, 51% and 16.2%, respectively. The antigen-binding avidity of IgG antibodies to PvMSP-1
19 was measured in sero-positive sera and the high-avidity of IgG, IgG1 and IgG3 was found in 66.6%, 61% and 47% of the infected subjects with
P. vivax, respectively. The present result shows that individuals who exposed to vivax malaria in the endemic region in Iran develop antibodies with high-avidity to PvMSP-1
19. These results could help to understand the interactions between the host and
P. vivax parasite in development of MSP-1
19-based vaccine. |
---|---|
AbstractList | The C-terminal region of
Plasmodium vivax merozoite surface protein 1 (PvMSP-1
19) is a leading vaccine candidate for inclusion in a polyvalent malaria vaccine. In the present study, the IgG subclasses profile and the avidity of IgG to PvMSP-1
19 were evaluated in individuals (
n
=
94) naturally exposed to
P. vivax parasite in malaria endemic areas in Chabahar districts, Iran. In individuals with patent
P. vivax malaria, 86.1% was sero-positive to PvMSP-1
19 and IgG1 (81.9%) was the predominant subclass. In addition, to determine the persistence of specific IgG, IgG1 and IgG3 antibodies to PvMSP-1
19, the frequency of antibodies was determined in the infected subjects (
n
=
74) after treatment with standard chloroquine and it was detected that the frequency of responders was significantly reduced to 51.3%, 51% and 16.2%, respectively. The antigen-binding avidity of IgG antibodies to PvMSP-1
19 was measured in sero-positive sera and the high-avidity of IgG, IgG1 and IgG3 was found in 66.6%, 61% and 47% of the infected subjects with
P. vivax, respectively. The present result shows that individuals who exposed to vivax malaria in the endemic region in Iran develop antibodies with high-avidity to PvMSP-1
19. These results could help to understand the interactions between the host and
P. vivax parasite in development of MSP-1
19-based vaccine. The C-terminal region of Plasmodium vivax merozoite surface protein 1 (PvMSP-1 sub(19)) is a leading vaccine candidate for inclusion in a polyvalent malaria vaccine. In the present study, the IgG subclasses profile and the avidity of IgG to PvMSP-1 sub(19) were evaluated in individuals (n = 94) naturally exposed to P. vivax parasite in malaria endemic areas in Chabahar districts, Iran. In individuals with patent P. vivax malaria, 86.1% was sero-positive to PvMSP-1 sub(19) and IgG1 (81.9%) was the predominant subclass. In addition, to determine the persistence of specific IgG, IgG1 and IgG3 antibodies to PvMSP- 1 sub(19), the frequency of antibodies was determined in the infected subjects (n = 74) after treatment with standard chloroquine and it was detected that the frequency of responders was significantly reduced to 51.3%, 51% and 16.2%, respectively. The antigen-binding avidity of IgG antibodies to PvMSP-1 sub(19) was measured in sero-positive sera and the high-avidity of IgG, IgG1 and IgG3 was found in 66.6%, 61% and 47% of the infected subjects with P. vivax, respectively. The present result shows that individuals who exposed to vivax malaria in the endemic region in Iran develop antibodies with high-avidity to PvMSP-1 sub(19). These results could help to understand the interactions between the host and P. vivax parasite in development of MSP-1 sub(19)-based vaccine. The C-terminal region of Plasmodium vivax merozoite surface protein 1 (PvMSP-1(19)) is a leading vaccine candidate for inclusion in a polyvalent malaria vaccine. In the present study, the IgG subclasses profile and the avidity of IgG to PvMSP-1(19) were evaluated in individuals (n=94) naturally exposed to P. vivax parasite in malaria endemic areas in Chabahar districts, Iran. In individuals with patent P. vivax malaria, 86.1% was sero-positive to PvMSP-1(19) and IgG1 (81.9%) was the predominant subclass. In addition, to determine the persistence of specific IgG, IgG1 and IgG3 antibodies to PvMSP-1(19), the frequency of antibodies was determined in the infected subjects (n=74) after treatment with standard chloroquine and it was detected that the frequency of responders was significantly reduced to 51.3%, 51% and 16.2%, respectively. The antigen-binding avidity of IgG antibodies to PvMSP-1(19) was measured in sero-positive sera and the high-avidity of IgG, IgG1 and IgG3 was found in 66.6%, 61% and 47% of the infected subjects with P. vivax, respectively. The present result shows that individuals who exposed to vivax malaria in the endemic region in Iran develop antibodies with high-avidity to PvMSP-1(19). These results could help to understand the interactions between the host and P. vivax parasite in development of MSP-1(19)-based vaccine.The C-terminal region of Plasmodium vivax merozoite surface protein 1 (PvMSP-1(19)) is a leading vaccine candidate for inclusion in a polyvalent malaria vaccine. In the present study, the IgG subclasses profile and the avidity of IgG to PvMSP-1(19) were evaluated in individuals (n=94) naturally exposed to P. vivax parasite in malaria endemic areas in Chabahar districts, Iran. In individuals with patent P. vivax malaria, 86.1% was sero-positive to PvMSP-1(19) and IgG1 (81.9%) was the predominant subclass. In addition, to determine the persistence of specific IgG, IgG1 and IgG3 antibodies to PvMSP-1(19), the frequency of antibodies was determined in the infected subjects (n=74) after treatment with standard chloroquine and it was detected that the frequency of responders was significantly reduced to 51.3%, 51% and 16.2%, respectively. The antigen-binding avidity of IgG antibodies to PvMSP-1(19) was measured in sero-positive sera and the high-avidity of IgG, IgG1 and IgG3 was found in 66.6%, 61% and 47% of the infected subjects with P. vivax, respectively. The present result shows that individuals who exposed to vivax malaria in the endemic region in Iran develop antibodies with high-avidity to PvMSP-1(19). These results could help to understand the interactions between the host and P. vivax parasite in development of MSP-1(19)-based vaccine. The C-terminal region of Plasmodium vivax merozoite surface protein 1 (PvMSP-1(19)) is a leading vaccine candidate for inclusion in a polyvalent malaria vaccine. In the present study, the IgG subclasses profile and the avidity of IgG to PvMSP-1(19) were evaluated in individuals (n=94) naturally exposed to P. vivax parasite in malaria endemic areas in Chabahar districts, Iran. In individuals with patent P. vivax malaria, 86.1% was sero-positive to PvMSP-1(19) and IgG1 (81.9%) was the predominant subclass. In addition, to determine the persistence of specific IgG, IgG1 and IgG3 antibodies to PvMSP-1(19), the frequency of antibodies was determined in the infected subjects (n=74) after treatment with standard chloroquine and it was detected that the frequency of responders was significantly reduced to 51.3%, 51% and 16.2%, respectively. The antigen-binding avidity of IgG antibodies to PvMSP-1(19) was measured in sero-positive sera and the high-avidity of IgG, IgG1 and IgG3 was found in 66.6%, 61% and 47% of the infected subjects with P. vivax, respectively. The present result shows that individuals who exposed to vivax malaria in the endemic region in Iran develop antibodies with high-avidity to PvMSP-1(19). These results could help to understand the interactions between the host and P. vivax parasite in development of MSP-1(19)-based vaccine. |
Author | Salmanian, Ali-Hatef Mehrizi, Akram Abouie Zakeri, Sedigheh Sanati, Mohammad Hossein Djadid, Navid Dinparast |
Author_xml | – sequence: 1 givenname: Akram Abouie surname: Mehrizi fullname: Mehrizi, Akram Abouie organization: Malaria and Vector Research Group (MVRG), Biotechnology Research Center, Pasteur Institute of Iran, Pasteur Avenue, P.O. Box 1316943551, Tehran, Iran – sequence: 2 givenname: Sedigheh surname: Zakeri fullname: Zakeri, Sedigheh email: zakeris@yahoo.com, zakeris@pasteur.ac.ir organization: Malaria and Vector Research Group (MVRG), Biotechnology Research Center, Pasteur Institute of Iran, Pasteur Avenue, P.O. Box 1316943551, Tehran, Iran – sequence: 3 givenname: Ali-Hatef surname: Salmanian fullname: Salmanian, Ali-Hatef organization: National Research Center for Genetic Engineering and Biotechnology, Tehran, Iran – sequence: 4 givenname: Mohammad Hossein surname: Sanati fullname: Sanati, Mohammad Hossein organization: National Research Center for Genetic Engineering and Biotechnology, Tehran, Iran – sequence: 5 givenname: Navid Dinparast surname: Djadid fullname: Djadid, Navid Dinparast organization: Malaria and Vector Research Group (MVRG), Biotechnology Research Center, Pasteur Institute of Iran, Pasteur Avenue, P.O. Box 1316943551, Tehran, Iran |
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CitedBy_id | crossref_primary_10_1007_s00436_011_2370_z crossref_primary_10_1016_j_actatropica_2011_04_012 crossref_primary_10_1111_j_1365_3024_2011_01331_x crossref_primary_10_1186_1475_2875_11_86 crossref_primary_10_1186_s12936_020_03243_3 crossref_primary_10_1097_INF_0b013e31822d1451 crossref_primary_10_1186_1475_2875_11_126 crossref_primary_10_1007_s00436_011_2413_5 crossref_primary_10_1128_IAI_00522_20 crossref_primary_10_1016_j_actatropica_2017_05_026 crossref_primary_10_1007_s00430_018_0535_4 crossref_primary_10_1016_j_actatropica_2018_12_014 crossref_primary_10_1016_j_mimet_2016_02_003 crossref_primary_10_1016_j_micinf_2014_02_002 crossref_primary_10_7717_peerj_17632 crossref_primary_10_1371_journal_pone_0151900 crossref_primary_10_2196_15690 crossref_primary_10_1371_journal_pone_0148723 crossref_primary_10_3347_kjp_2012_50_1_15 crossref_primary_10_1017_S0031182015000670 crossref_primary_10_1021_pr100705g crossref_primary_10_1186_s12936_015_0547_0 |
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Keywords | Plasmodium vivax Avidity Immune response Malaria C-terminal region of MSP-1 Antibody Protozoa Apicomplexa Protozoal disease IgG Parasitosis Infection Tropical medicine Merozoite surface protein-1 |
Language | English |
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Snippet | The C-terminal region of
Plasmodium vivax merozoite surface protein 1 (PvMSP-1
19) is a leading vaccine candidate for inclusion in a polyvalent malaria... The C-terminal region of Plasmodium vivax merozoite surface protein 1 (PvMSP-1(19)) is a leading vaccine candidate for inclusion in a polyvalent malaria... The C-terminal region of Plasmodium vivax merozoite surface protein 1 (PvMSP-1 sub(19)) is a leading vaccine candidate for inclusion in a polyvalent malaria... |
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SubjectTerms | Adolescent Adult Aged Animals Antibodies, Protozoan Antibodies, Protozoan - blood Antibodies, Protozoan - classification Antibody Antibody Affinity Avidity Biological and medical sciences C-terminal region of MSP-1 Child Child, Preschool Endemic Diseases Female General aspects Genetics Human protozoal diseases Humans Immune response Immunoglobulin G Immunoglobulin G - blood Immunoglobulin G - classification Infant Infectious diseases Iran Iran - epidemiology Life Sciences Malaria Malaria, Vivax Malaria, Vivax - epidemiology Malaria, Vivax - immunology Male Medical sciences Merozoite Surface Protein 1 Merozoite Surface Protein 1 - immunology Middle Aged Parasitic diseases Plasmodium vivax Plasmodium vivax - immunology Protozoal diseases Young Adult |
Title | IgG subclasses pattern and high-avidity antibody to the C-terminal region of merozoite surface protein 1 of Plasmodium vivax in an unstable hypoendemic region in Iran |
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