Charles Nkansah, Felix Osei-Boakye, Gabriel Abbam, Samuel K. Appiah, Charles A. Derigubah, Simon B. Bani, Samira Daud, Emmanuel K. Alhassan, Isaac Adjei, Emmanuel Appiah-Kubi, Anastasia Koduah, Bright Boakye, Samsiyatu Abdulai, Neena I. Anass, Dorcas Serwaa, Boniface N. Ukwah, Victor U. Usanga, Ejike F. Chukwurah
{"title":"恶性疟原虫红细胞膜蛋白-1特异性结构域抗体及其与预防严重疟疾性贫血的关系:加纳儿童前瞻性研究。","authors":"Charles Nkansah, Felix Osei-Boakye, Gabriel Abbam, Samuel K. Appiah, Charles A. Derigubah, Simon B. Bani, Samira Daud, Emmanuel K. Alhassan, Isaac Adjei, Emmanuel Appiah-Kubi, Anastasia Koduah, Bright Boakye, Samsiyatu Abdulai, Neena I. Anass, Dorcas Serwaa, Boniface N. Ukwah, Victor U. Usanga, Ejike F. Chukwurah","doi":"10.1002/hsr2.70123","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p><i>Plasmodium falciparum</i> erythrocyte membrane protein-1 (<i>Pf</i>EMP-1) is important in malaria pathogenicity as it mediates <i>Pf</i>-infected erythrocytes cytoadherence to host endothelial microvasculature receptors. Naturally acquired antibodies against specific <i>Pf</i>EMP-1 antigens may be beneficial in clinical malaria protection. This study determined antibodies to DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains of <i>Pf</i>EMP-1 in children with <i>P. falciparum</i> malaria in Tamale, Ghana.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Sixty <i>P. falciparum</i>-infected children, and 30 controls, aged 1–12 years were recruited for this case-control study from April to July 2023 in Northern Ghana. Participants with uncomplicated malaria had asexual <i>P. falciparum</i> in peripheral blood and Hb ≥ 5.0 g/dL, and severe malaria was diagnosed when participants had Hb < 5.0 g/dL in addition to asexual <i>P. falciparum</i> in peripheral blood. Blood cell indices were measured using hematology analyzer, and IgG antibodies to DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains of <i>Pf</i>EMP-1 and pro-inflammatory cytokines were detected using enzyme-linked immunosorbent assay. Data were analyzed using SPSS version 26.0.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The prevalence of <i>Pf</i>EMP-1 IgG antibodies among <i>P. falciparum</i>-infected children and the uninfected group was 65.0% and 6.7%, respectively. <i>Pf</i>EMP-1 IgG antibodies were present in 83.3% of uncomplicated malaria cases, and 46.7% in severe malaria subjects. Plasma levels of <i>Pf</i>EMP-1 IgG antibodies were elevated in participants with uncomplicated malaria compared to those with severe malaria (<i>p</i> < 0.001). Hemoglobin, RBC, HCT, and platelet were significantly lower among <i>P. falciparum</i>-infected children without <i>Pf</i>EMP-1 IgG antibodies than among those with the antibodies. Prevalence of anemia among children with <i>Pf</i>EMP-1 IgG antibodies and those without the antibodies were 74.4% and 100%, respectively.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>The high prevalence of <i>Pf</i>EMP-1 IgG antibodies to DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains observed in participants with uncomplicated malaria, and the relationship between <i>Pf</i>EMP-1 IgG antibodies and blood cell parameters could indicate that the antibodies may be related to effective erythropoietic response in <i>P. falciparum</i> malaria. Immune antibodies against DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains of <i>Pf</i>EMP-1 may suppress the deteriorating effects of <i>Pf</i>EMP-1 antigens and provide immune protection against severe malarial anemia in children.</p>\n </section>\n </div>","PeriodicalId":36518,"journal":{"name":"Health Science Reports","volume":"7 10","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11462291/pdf/","citationCount":"0","resultStr":"{\"title\":\"Antibodies to specific domains of Plasmodium falciparum erythrocyte membrane protein-1 and its relationship with protection from severe malarial anemia: A prospective study among Ghanaian children\",\"authors\":\"Charles Nkansah, Felix Osei-Boakye, Gabriel Abbam, Samuel K. Appiah, Charles A. Derigubah, Simon B. Bani, Samira Daud, Emmanuel K. Alhassan, Isaac Adjei, Emmanuel Appiah-Kubi, Anastasia Koduah, Bright Boakye, Samsiyatu Abdulai, Neena I. Anass, Dorcas Serwaa, Boniface N. Ukwah, Victor U. Usanga, Ejike F. Chukwurah\",\"doi\":\"10.1002/hsr2.70123\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p><i>Plasmodium falciparum</i> erythrocyte membrane protein-1 (<i>Pf</i>EMP-1) is important in malaria pathogenicity as it mediates <i>Pf</i>-infected erythrocytes cytoadherence to host endothelial microvasculature receptors. Naturally acquired antibodies against specific <i>Pf</i>EMP-1 antigens may be beneficial in clinical malaria protection. This study determined antibodies to DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains of <i>Pf</i>EMP-1 in children with <i>P. falciparum</i> malaria in Tamale, Ghana.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Sixty <i>P. falciparum</i>-infected children, and 30 controls, aged 1–12 years were recruited for this case-control study from April to July 2023 in Northern Ghana. Participants with uncomplicated malaria had asexual <i>P. falciparum</i> in peripheral blood and Hb ≥ 5.0 g/dL, and severe malaria was diagnosed when participants had Hb < 5.0 g/dL in addition to asexual <i>P. falciparum</i> in peripheral blood. Blood cell indices were measured using hematology analyzer, and IgG antibodies to DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains of <i>Pf</i>EMP-1 and pro-inflammatory cytokines were detected using enzyme-linked immunosorbent assay. Data were analyzed using SPSS version 26.0.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>The prevalence of <i>Pf</i>EMP-1 IgG antibodies among <i>P. falciparum</i>-infected children and the uninfected group was 65.0% and 6.7%, respectively. <i>Pf</i>EMP-1 IgG antibodies were present in 83.3% of uncomplicated malaria cases, and 46.7% in severe malaria subjects. Plasma levels of <i>Pf</i>EMP-1 IgG antibodies were elevated in participants with uncomplicated malaria compared to those with severe malaria (<i>p</i> < 0.001). Hemoglobin, RBC, HCT, and platelet were significantly lower among <i>P. falciparum</i>-infected children without <i>Pf</i>EMP-1 IgG antibodies than among those with the antibodies. Prevalence of anemia among children with <i>Pf</i>EMP-1 IgG antibodies and those without the antibodies were 74.4% and 100%, respectively.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>The high prevalence of <i>Pf</i>EMP-1 IgG antibodies to DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains observed in participants with uncomplicated malaria, and the relationship between <i>Pf</i>EMP-1 IgG antibodies and blood cell parameters could indicate that the antibodies may be related to effective erythropoietic response in <i>P. falciparum</i> malaria. Immune antibodies against DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains of <i>Pf</i>EMP-1 may suppress the deteriorating effects of <i>Pf</i>EMP-1 antigens and provide immune protection against severe malarial anemia in children.</p>\\n </section>\\n </div>\",\"PeriodicalId\":36518,\"journal\":{\"name\":\"Health Science Reports\",\"volume\":\"7 10\",\"pages\":\"\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-10-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11462291/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Health Science Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/hsr2.70123\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Health Science Reports","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/hsr2.70123","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
Antibodies to specific domains of Plasmodium falciparum erythrocyte membrane protein-1 and its relationship with protection from severe malarial anemia: A prospective study among Ghanaian children
Background
Plasmodium falciparum erythrocyte membrane protein-1 (PfEMP-1) is important in malaria pathogenicity as it mediates Pf-infected erythrocytes cytoadherence to host endothelial microvasculature receptors. Naturally acquired antibodies against specific PfEMP-1 antigens may be beneficial in clinical malaria protection. This study determined antibodies to DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains of PfEMP-1 in children with P. falciparum malaria in Tamale, Ghana.
Methods
Sixty P. falciparum-infected children, and 30 controls, aged 1–12 years were recruited for this case-control study from April to July 2023 in Northern Ghana. Participants with uncomplicated malaria had asexual P. falciparum in peripheral blood and Hb ≥ 5.0 g/dL, and severe malaria was diagnosed when participants had Hb < 5.0 g/dL in addition to asexual P. falciparum in peripheral blood. Blood cell indices were measured using hematology analyzer, and IgG antibodies to DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains of PfEMP-1 and pro-inflammatory cytokines were detected using enzyme-linked immunosorbent assay. Data were analyzed using SPSS version 26.0.
Results
The prevalence of PfEMP-1 IgG antibodies among P. falciparum-infected children and the uninfected group was 65.0% and 6.7%, respectively. PfEMP-1 IgG antibodies were present in 83.3% of uncomplicated malaria cases, and 46.7% in severe malaria subjects. Plasma levels of PfEMP-1 IgG antibodies were elevated in participants with uncomplicated malaria compared to those with severe malaria (p < 0.001). Hemoglobin, RBC, HCT, and platelet were significantly lower among P. falciparum-infected children without PfEMP-1 IgG antibodies than among those with the antibodies. Prevalence of anemia among children with PfEMP-1 IgG antibodies and those without the antibodies were 74.4% and 100%, respectively.
Conclusion
The high prevalence of PfEMP-1 IgG antibodies to DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains observed in participants with uncomplicated malaria, and the relationship between PfEMP-1 IgG antibodies and blood cell parameters could indicate that the antibodies may be related to effective erythropoietic response in P. falciparum malaria. Immune antibodies against DBLα2, CIDRα1, DBLβ12, and DBLγ6 domains of PfEMP-1 may suppress the deteriorating effects of PfEMP-1 antigens and provide immune protection against severe malarial anemia in children.