Eliud O Odhiambo, Kagan A Mellencamp, Prasida Holla, George Ayodo, Chandy C John
The authors of studies in high-malaria transmission areas have associated the opsonic phagocytosis (OP) of merozoites with protection from clinical malaria; however, OP studies have not been conducted in low transmission areas. In the current study, blood samples were collected from 5,753 individuals in a Kenyan highland area of low, unstable transmission in 2007 and monitored for clinical malaria through 2017. In a nested case-control design, individuals who developed clinical malaria (cases, N = 317) were matched 1:1 by age and village with those who did not (controls, N = 317). A novel OP assay was developed, and the association of OP with the risk of clinical malaria and IgG responses to Plasmodium falciparum antigens in individuals <5 years old, 5-14 years old, and ≥15 years old was examined. Opsonic phagocytosis levels increased with age; however, the proportion of individuals who tested positive for an OP response was <50% until individuals were ≥15 years old. After adjustment for potential confounding factors, OP levels were associated with an increased risk of clinical malaria in individuals 5-14 years old (adjusted odds ratio: 3.32 [CI: 1.13-9.77]) and ≥15 years old (adjusted odds ratio: 4.85 [CI: 1.02-23.00]), but not in children <5 years old (adjusted odds ratio: 0.57 [CI: 0.20-1.64]). In this low-malaria transmission area, OP responses did not develop in most individuals until they were ≥15 years old, and OP levels in individuals ≥5 years old were associated with an increased risk of clinical malaria, potentially reflecting that OP levels are markers of malaria exposure, providing additional information beyond standard geographic and intervention-based risk markers.
{"title":"A Novel Phagocytosis Assay Reveals the Association between Elevated Opsonic Phagocytosis Levels and an Increased Risk of Clinical Malaria in a Low-Malaria Transmission Area.","authors":"Eliud O Odhiambo, Kagan A Mellencamp, Prasida Holla, George Ayodo, Chandy C John","doi":"10.4269/ajtmh.25-0349","DOIUrl":"10.4269/ajtmh.25-0349","url":null,"abstract":"<p><p>The authors of studies in high-malaria transmission areas have associated the opsonic phagocytosis (OP) of merozoites with protection from clinical malaria; however, OP studies have not been conducted in low transmission areas. In the current study, blood samples were collected from 5,753 individuals in a Kenyan highland area of low, unstable transmission in 2007 and monitored for clinical malaria through 2017. In a nested case-control design, individuals who developed clinical malaria (cases, N = 317) were matched 1:1 by age and village with those who did not (controls, N = 317). A novel OP assay was developed, and the association of OP with the risk of clinical malaria and IgG responses to Plasmodium falciparum antigens in individuals <5 years old, 5-14 years old, and ≥15 years old was examined. Opsonic phagocytosis levels increased with age; however, the proportion of individuals who tested positive for an OP response was <50% until individuals were ≥15 years old. After adjustment for potential confounding factors, OP levels were associated with an increased risk of clinical malaria in individuals 5-14 years old (adjusted odds ratio: 3.32 [CI: 1.13-9.77]) and ≥15 years old (adjusted odds ratio: 4.85 [CI: 1.02-23.00]), but not in children <5 years old (adjusted odds ratio: 0.57 [CI: 0.20-1.64]). In this low-malaria transmission area, OP responses did not develop in most individuals until they were ≥15 years old, and OP levels in individuals ≥5 years old were associated with an increased risk of clinical malaria, potentially reflecting that OP levels are markers of malaria exposure, providing additional information beyond standard geographic and intervention-based risk markers.</p>","PeriodicalId":7752,"journal":{"name":"American Journal of Tropical Medicine and Hygiene","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676608/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145257131","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sooyoung Kim, Betty Nabukeera, Yehu Taremwa, Maureen Ng'etich, Flavian Otieno, Steve Cygu, Dan Kajungu, Agnes Kiragga, Yesim Tozan
Climate change is anticipated to significantly affect malaria transmission. Previous research has shown lagged, nonlinear associations between climate variables and malaria risk, with highly context-specific exposure-lag-response relationship. Using weekly malaria case data collected between July 2018 and February 2023 from a health facility within the Iganga-Mayuge Health and Demographic Surveillance System site in Uganda and remotely sensed temperature and rainfall data, we quantified the associations between temperature and rainfall and risk of developing symptomatic malaria using a distributed lag nonlinear model. Furthermore, we investigated whether these associations varied by age group. Our analysis revealed a lag of 2 to 8 weeks between exposure to rainfall exceeding 200 mm/week and a significant increase in the risk of developing symptomatic malaria; no statistically significant lagged association was found with temperature. Additionally, the risk in school-aged children was less sensitive to climate variables compared with the other age groups. Rainfall was found to be associated with an increased risk at a lag of 2 months at the study site. This finding provides valuable guidance for local health authorities in determining the optimal timing for preventive interventions and in preparing for the anticipated rise in demand for malaria case management. The observed variations in the risk of developing symptomatic malaria across different age groups highlight the need for targeted interventions tailored to specific populations. Overall, the significant associations between climate variables and malaria risk underscore the importance of context-specific, adaptive malaria control strategies, complemented by broader efforts to mitigate climate change.
{"title":"Quantifying the Lagged Effects of Climate Variables on Malaria Risk in Eastern Uganda.","authors":"Sooyoung Kim, Betty Nabukeera, Yehu Taremwa, Maureen Ng'etich, Flavian Otieno, Steve Cygu, Dan Kajungu, Agnes Kiragga, Yesim Tozan","doi":"10.4269/ajtmh.25-0031","DOIUrl":"10.4269/ajtmh.25-0031","url":null,"abstract":"<p><p>Climate change is anticipated to significantly affect malaria transmission. Previous research has shown lagged, nonlinear associations between climate variables and malaria risk, with highly context-specific exposure-lag-response relationship. Using weekly malaria case data collected between July 2018 and February 2023 from a health facility within the Iganga-Mayuge Health and Demographic Surveillance System site in Uganda and remotely sensed temperature and rainfall data, we quantified the associations between temperature and rainfall and risk of developing symptomatic malaria using a distributed lag nonlinear model. Furthermore, we investigated whether these associations varied by age group. Our analysis revealed a lag of 2 to 8 weeks between exposure to rainfall exceeding 200 mm/week and a significant increase in the risk of developing symptomatic malaria; no statistically significant lagged association was found with temperature. Additionally, the risk in school-aged children was less sensitive to climate variables compared with the other age groups. Rainfall was found to be associated with an increased risk at a lag of 2 months at the study site. This finding provides valuable guidance for local health authorities in determining the optimal timing for preventive interventions and in preparing for the anticipated rise in demand for malaria case management. The observed variations in the risk of developing symptomatic malaria across different age groups highlight the need for targeted interventions tailored to specific populations. Overall, the significant associations between climate variables and malaria risk underscore the importance of context-specific, adaptive malaria control strategies, complemented by broader efforts to mitigate climate change.</p>","PeriodicalId":7752,"journal":{"name":"American Journal of Tropical Medicine and Hygiene","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676583/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145243363","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Joby Robleto-Quesada, Esteban Jara-Segura, José-Ricardo Montenegro, Marcos Mauricio Siliezar-Tala, María Jose Suárez-Sánchez, Juan José Madrigal-Sánchez
Sickle cell trait carriers are generally considered asymptomatic; nevertheless, there are potential complications. The spleen is vulnerable to infarction because of its role in trapping and removing sickle cells and its hypoxic environment. In this report, a case of a 31-year-old physically active man who experienced severe abdominal pain near the peak of the Acatenango Volcano in Guatemala is described. At the hospital, he was diagnosed with splenic infarction, requiring splenectomy. Pathological analysis of the spleen revealed interstitial hemorrhage and marked congestion of capillaries by sickle-shaped erythrocytes. Laboratory studies revealed no evidence of anemia or any alteration in the red blood cell formula; however, leukocytosis was observed at the time of the event, which rapidly decreased on subsequent days. In contrast, platelets increased after the spleen removal. Capillary electrophoresis revealed the sickle cell carrier state. Genetic alterations associated with thrombophilia, alpha thalassemia, and other beta globin hemoglobinopathies were absent. This case reinforces evidence that high-altitude hypoxia can trigger sickle cell formation in heterozygous carriers and lead to splenic damage.
{"title":"Histopathologic and Molecular Evidence of Splenic Infarction Associated with Sickle Cell Trait: An Instructive Case in Central America.","authors":"Joby Robleto-Quesada, Esteban Jara-Segura, José-Ricardo Montenegro, Marcos Mauricio Siliezar-Tala, María Jose Suárez-Sánchez, Juan José Madrigal-Sánchez","doi":"10.4269/ajtmh.25-0227","DOIUrl":"10.4269/ajtmh.25-0227","url":null,"abstract":"<p><p>Sickle cell trait carriers are generally considered asymptomatic; nevertheless, there are potential complications. The spleen is vulnerable to infarction because of its role in trapping and removing sickle cells and its hypoxic environment. In this report, a case of a 31-year-old physically active man who experienced severe abdominal pain near the peak of the Acatenango Volcano in Guatemala is described. At the hospital, he was diagnosed with splenic infarction, requiring splenectomy. Pathological analysis of the spleen revealed interstitial hemorrhage and marked congestion of capillaries by sickle-shaped erythrocytes. Laboratory studies revealed no evidence of anemia or any alteration in the red blood cell formula; however, leukocytosis was observed at the time of the event, which rapidly decreased on subsequent days. In contrast, platelets increased after the spleen removal. Capillary electrophoresis revealed the sickle cell carrier state. Genetic alterations associated with thrombophilia, alpha thalassemia, and other beta globin hemoglobinopathies were absent. This case reinforces evidence that high-altitude hypoxia can trigger sickle cell formation in heterozygous carriers and lead to splenic damage.</p>","PeriodicalId":7752,"journal":{"name":"American Journal of Tropical Medicine and Hygiene","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676613/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145243389","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Victoria Pando-Robles, Julio Alvarez-Obregón, Guadalupe Díaz Del Castillo-Flores, Jesús Felipe González-Roldán, Eric Saúl Raga-Sarabia, Cassandra González-Acosta, Jorge Fernando Méndez-Galván
Dengue is the most prevalent arboviral disease worldwide. This study aimed to describe the epidemiological and economic burden of dengue in Mexico by identifying comorbidities and conditions associated with clinical outcomes. A retrospective analysis of dengue epidemiological data in Mexico from 2010 to 2020 was conducted using surveillance system databases (Sistema Nacional de Vigilancia Epidemiológica and Sistema Único de Información para la Vigilancia Epidemiológica). Data on probable, laboratory-confirmed, outpatient, and hospitalized cases as well as deaths were collected along with comorbidities and pregnancy status; a survey was conducted to gather information on health care resources utilization. Sistema Nacional de Vigilancia Epidemiológica recorded 1,620,872 cases, among which there were 336,991 laboratory-confirmed cases, 110,437 hospitalizations, and 1,385 deaths. The hospitalization fatality rate increased from 0.72% to 2.6%. Age distribution of severe dengue shifted from predominantly affecting individuals 10-24 years old (2010-2016) to those 0-19 years old (2017-2020). These findings highlight the need for age-specific health care interventions. Comorbidities, such as diabetes, liver cirrhosis, hypertension, kidney disease, and hematological disorders, and pregnancy were significantly associated with an increased risk of hospitalization and mortality. Additionally, peptic ulcer was associated with a higher risk of hospitalization. The estimated annual medical cost during outbreak was U.S. $111,851,376 (2019, 211.0 [case] incidence) in contrast to pre-/postoutbreak, with total costs of U.S. $23,713,589 (2018, 62.4 [case] incidence) and U.S. $39,780,809 (2020, 94.1 [case] incidence), respectively. The robustness of collected data contributes to more comprehensive understanding of the public health implications of dengue, particularly during outbreaks.
登革热是世界上最流行的虫媒病毒性疾病。本研究旨在通过确定与临床结果相关的合并症和条件来描述墨西哥登革热的流行病学和经济负担。利用监测系统数据库(Sistema Nacional de Vigilancia Epidemiológica和Sistema Único de Información para la Vigilancia Epidemiológica)对2010 - 2020年墨西哥登革热流行病学数据进行了回顾性分析。收集了有关可能病例、实验室确诊病例、门诊病例和住院病例以及死亡的数据,并收集了合并症和妊娠状况的数据;开展了一项调查,以收集有关卫生保健资源利用的信息。全国维持治安系统Epidemiológica记录了1,620,872例病例,其中有336,991例实验室确诊病例,110437例住院治疗,1,385例死亡。住院死亡率从0.72%上升到2.6%。严重登革热的年龄分布从主要影响10-24岁个体(2010-2016年)转变为主要影响0-19岁个体(2017-2020年)。这些发现突出了针对特定年龄的卫生保健干预措施的必要性。合并症,如糖尿病、肝硬化、高血压、肾病和血液系统疾病,以及妊娠与住院和死亡风险增加显著相关。此外,消化性溃疡与较高的住院风险相关。与爆发前/爆发后相比,疫情期间的年医疗费用估计为111,851,376美元(2019年,211.0例发病率),总费用分别为23,713,589美元(2018年,62.4例发病率)和39,780,809美元(2020年,94.1例发病率)。所收集数据的可靠性有助于更全面地了解登革热对公共卫生的影响,特别是在疫情期间。
{"title":"Epidemiological and Economic Burden of Dengue in Mexico: Data Analysis from 2010 to 2020.","authors":"Victoria Pando-Robles, Julio Alvarez-Obregón, Guadalupe Díaz Del Castillo-Flores, Jesús Felipe González-Roldán, Eric Saúl Raga-Sarabia, Cassandra González-Acosta, Jorge Fernando Méndez-Galván","doi":"10.4269/ajtmh.24-0777","DOIUrl":"10.4269/ajtmh.24-0777","url":null,"abstract":"<p><p>Dengue is the most prevalent arboviral disease worldwide. This study aimed to describe the epidemiological and economic burden of dengue in Mexico by identifying comorbidities and conditions associated with clinical outcomes. A retrospective analysis of dengue epidemiological data in Mexico from 2010 to 2020 was conducted using surveillance system databases (Sistema Nacional de Vigilancia Epidemiológica and Sistema Único de Información para la Vigilancia Epidemiológica). Data on probable, laboratory-confirmed, outpatient, and hospitalized cases as well as deaths were collected along with comorbidities and pregnancy status; a survey was conducted to gather information on health care resources utilization. Sistema Nacional de Vigilancia Epidemiológica recorded 1,620,872 cases, among which there were 336,991 laboratory-confirmed cases, 110,437 hospitalizations, and 1,385 deaths. The hospitalization fatality rate increased from 0.72% to 2.6%. Age distribution of severe dengue shifted from predominantly affecting individuals 10-24 years old (2010-2016) to those 0-19 years old (2017-2020). These findings highlight the need for age-specific health care interventions. Comorbidities, such as diabetes, liver cirrhosis, hypertension, kidney disease, and hematological disorders, and pregnancy were significantly associated with an increased risk of hospitalization and mortality. Additionally, peptic ulcer was associated with a higher risk of hospitalization. The estimated annual medical cost during outbreak was U.S. $111,851,376 (2019, 211.0 [case] incidence) in contrast to pre-/postoutbreak, with total costs of U.S. $23,713,589 (2018, 62.4 [case] incidence) and U.S. $39,780,809 (2020, 94.1 [case] incidence), respectively. The robustness of collected data contributes to more comprehensive understanding of the public health implications of dengue, particularly during outbreaks.</p>","PeriodicalId":7752,"journal":{"name":"American Journal of Tropical Medicine and Hygiene","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676618/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145243402","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Bastien Bigeard, Loïc Epelboin, Pierre-Marie Roger, Sylvaine Bastian, Lucas Maisonobe, Narcisse Elenga, Amadou Balde, Vincent Sainte-Rose, Loïc Raffray, Olivier Belmonte, Renaud Blondé, Louis Collet, André Cabié, Claude Olive
Chromobacterium violaceum is a Gram-negative bacillus found in soil and water in tropical and subtropical areas. Although usually nonpathogenic, it can cause severe infections in humans. Case series and literature reviews remain rare. In this study, we identified 26 cases that have occurred in French overseas territories (FOTs) since 1999 and reviewed 57 cases published over the past 20 years. The portal of entry was cutaneous for 53% of our patients and 38% of published cases, followed by pulmonary, digestive, mucosal, and urinary. None of our patients were immunocompromised. Nine of our patients were hospitalized in intensive care, including five deaths (19%). In the case review, 26 patients died (46%), four of whom were immunocompromised. Most of the strains were sensitive to ciprofloxacin (FOT 100%, review 98%), cotrimoxazole (FOT 95%, review 94%), and imipenem (FOT 84%, review 92%).
{"title":"Infection with Chromobacterium violaceum in the Tropical and Subtropical French Overseas Territories of the Americas and the Indian Ocean: A Case-Series and Review.","authors":"Bastien Bigeard, Loïc Epelboin, Pierre-Marie Roger, Sylvaine Bastian, Lucas Maisonobe, Narcisse Elenga, Amadou Balde, Vincent Sainte-Rose, Loïc Raffray, Olivier Belmonte, Renaud Blondé, Louis Collet, André Cabié, Claude Olive","doi":"10.4269/ajtmh.23-0340","DOIUrl":"10.4269/ajtmh.23-0340","url":null,"abstract":"<p><p>Chromobacterium violaceum is a Gram-negative bacillus found in soil and water in tropical and subtropical areas. Although usually nonpathogenic, it can cause severe infections in humans. Case series and literature reviews remain rare. In this study, we identified 26 cases that have occurred in French overseas territories (FOTs) since 1999 and reviewed 57 cases published over the past 20 years. The portal of entry was cutaneous for 53% of our patients and 38% of published cases, followed by pulmonary, digestive, mucosal, and urinary. None of our patients were immunocompromised. Nine of our patients were hospitalized in intensive care, including five deaths (19%). In the case review, 26 patients died (46%), four of whom were immunocompromised. Most of the strains were sensitive to ciprofloxacin (FOT 100%, review 98%), cotrimoxazole (FOT 95%, review 94%), and imipenem (FOT 84%, review 92%).</p>","PeriodicalId":7752,"journal":{"name":"American Journal of Tropical Medicine and Hygiene","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676609/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145243427","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Dengue fever is a common arboviral illness that can result in severe hemorrhagic complications, although spontaneous intraperitoneal bleeding remains rare. We report the case of a 26-year-old previously healthy female who presented with a 4-day history of high-grade fever and myalgia that was later diagnosed as dengue fever. During hospitalization, she developed vaginal bleeding followed by generalized abdominal pain and shock. Contrast-enhanced computed tomography revealed significant hemoperitoneum, despite a normal coagulation profile and no identifiable bleeding source. She was managed conservatively with supportive care and made a full recovery. A 1-year follow-up was unremarkable. This case underscores the importance of early recognition, prompt imaging, and consideration of differential diagnoses. In the absence of established guidelines for managing spontaneous intraperitoneal hemorrhage in dengue, individualized conservative treatment may be effective. Clinicians should remain vigilant for atypical presentations to ensure timely diagnosis and appropriate management.
{"title":"Conservative Treatment of Spontaneous Intraperitoneal Hemorrhage in Severe Dengue: A Case Report and Review.","authors":"Panita Looareesuwan, Chaisith Sivakorn, Viravarn Luvira","doi":"10.4269/ajtmh.25-0296","DOIUrl":"10.4269/ajtmh.25-0296","url":null,"abstract":"<p><p>Dengue fever is a common arboviral illness that can result in severe hemorrhagic complications, although spontaneous intraperitoneal bleeding remains rare. We report the case of a 26-year-old previously healthy female who presented with a 4-day history of high-grade fever and myalgia that was later diagnosed as dengue fever. During hospitalization, she developed vaginal bleeding followed by generalized abdominal pain and shock. Contrast-enhanced computed tomography revealed significant hemoperitoneum, despite a normal coagulation profile and no identifiable bleeding source. She was managed conservatively with supportive care and made a full recovery. A 1-year follow-up was unremarkable. This case underscores the importance of early recognition, prompt imaging, and consideration of differential diagnoses. In the absence of established guidelines for managing spontaneous intraperitoneal hemorrhage in dengue, individualized conservative treatment may be effective. Clinicians should remain vigilant for atypical presentations to ensure timely diagnosis and appropriate management.</p>","PeriodicalId":7752,"journal":{"name":"American Journal of Tropical Medicine and Hygiene","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676611/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145243354","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yaquta Nur Mohamud, Wanna Chaijaroenkul, Kesara Na-Bangchang
This systematic review examines the multifaceted roles of γδ T cells in malaria and tuberculosis (TB) with an emphasis on subset-specific dynamics and functional plasticity. In malaria, γδ T cells, particularly Vγ9Vδ2+ cells, are rapidly activated upon infection with Plasmodium falciparum, exerting antiparasitic effects through the production of proinflammatory cytokines, cytotoxicity, and immune modulation. However, chronic or repeated exposure to malaria leads to the functional exhaustion of Vδ2+ cells, which is characterized by reduced cytokine responsiveness and a shift toward regulatory phenotypes. In TB, γδ T cells contribute to pathogen containment through the secretion of interferon-γ and interleukin-17, the activation of macrophages, and the formation of granulomas. Yet, active TB is often associated with reduced peripheral γδ T-cell frequencies, possibly because of tissue migration or exhaustion. Emerging evidence also highlights distinct roles for CD8+ γδ T cells and Vδ1+ subsets in latent infection and local tissue immunity. Understanding the pathogen-specific and context-dependent functions of γδ T-cell subsets is critical for informing the development of targeted immunotherapies and vaccine strategies against malaria and TB.
{"title":"Exploring γδ T-Cell Responses in Malaria and Tuberculosis: Implications for Immunity, Coinfection, and Disease Management.","authors":"Yaquta Nur Mohamud, Wanna Chaijaroenkul, Kesara Na-Bangchang","doi":"10.4269/ajtmh.25-0316","DOIUrl":"10.4269/ajtmh.25-0316","url":null,"abstract":"<p><p>This systematic review examines the multifaceted roles of γδ T cells in malaria and tuberculosis (TB) with an emphasis on subset-specific dynamics and functional plasticity. In malaria, γδ T cells, particularly Vγ9Vδ2+ cells, are rapidly activated upon infection with Plasmodium falciparum, exerting antiparasitic effects through the production of proinflammatory cytokines, cytotoxicity, and immune modulation. However, chronic or repeated exposure to malaria leads to the functional exhaustion of Vδ2+ cells, which is characterized by reduced cytokine responsiveness and a shift toward regulatory phenotypes. In TB, γδ T cells contribute to pathogen containment through the secretion of interferon-γ and interleukin-17, the activation of macrophages, and the formation of granulomas. Yet, active TB is often associated with reduced peripheral γδ T-cell frequencies, possibly because of tissue migration or exhaustion. Emerging evidence also highlights distinct roles for CD8+ γδ T cells and Vδ1+ subsets in latent infection and local tissue immunity. Understanding the pathogen-specific and context-dependent functions of γδ T-cell subsets is critical for informing the development of targeted immunotherapies and vaccine strategies against malaria and TB.</p>","PeriodicalId":7752,"journal":{"name":"American Journal of Tropical Medicine and Hygiene","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676584/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145243376","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Echinococcosis is a zoonotic disease with global public health implications. However, its prevalence in Southeast Asia, including Myanmar, remains poorly documented. In this article, a case of human cystic echinococcosis caused by Echinococcus ortleppi (E. ortleppi) is reported in a 21-year-old man from Myanmar, who had traveled to Japan for vocational training. He presented to the study hospital in Tokyo after a chest radiograph revealed the presence of a giant cyst shadow in the right middle and lower lung fields. The cysts were excised, and echinococcosis was diagnosed on the basis of the pathological findings. Sequencing of a 150 base pair fragment of the mitochondrial cytochrome c oxidase subunit 1 gene in a section of cyst tissue was consistent with E. ortleppi. To the best of the authors' knowledge, this is the first documented case of human echinococcosis in Myanmar.
{"title":"A Human Case of Echinococcus ortleppi Infection in Myanmar.","authors":"Shundai Ko, Tatsuo Maeyashiki, Nana Fujita, Takeyuki Watadani, Yasuyuki Morishima, Reo Karakama, Satoshi Nagasaka, Masahiro Ishikane, Norio Ohmagari, Yutaro Akiyama","doi":"10.4269/ajtmh.25-0376","DOIUrl":"10.4269/ajtmh.25-0376","url":null,"abstract":"<p><p>Echinococcosis is a zoonotic disease with global public health implications. However, its prevalence in Southeast Asia, including Myanmar, remains poorly documented. In this article, a case of human cystic echinococcosis caused by Echinococcus ortleppi (E. ortleppi) is reported in a 21-year-old man from Myanmar, who had traveled to Japan for vocational training. He presented to the study hospital in Tokyo after a chest radiograph revealed the presence of a giant cyst shadow in the right middle and lower lung fields. The cysts were excised, and echinococcosis was diagnosed on the basis of the pathological findings. Sequencing of a 150 base pair fragment of the mitochondrial cytochrome c oxidase subunit 1 gene in a section of cyst tissue was consistent with E. ortleppi. To the best of the authors' knowledge, this is the first documented case of human echinococcosis in Myanmar.</p>","PeriodicalId":7752,"journal":{"name":"American Journal of Tropical Medicine and Hygiene","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676590/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145243680","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Accurate Leishmania species identification is crucial for epidemiological aspects and disease management. This study aimed to detect and identify the main causative species of human cutaneous and visceral leishmaniasis in Iran using nested polymerase chain reaction (PCR) based on size polymorphism of the ribosomal DNA (rDNA) intergenic region. In total, 180 clinical samples, including 156 confirmed positive cases, 24 confirmed negative cases, and 33 suspected cases that tested negative by microscopy, were collected from skin lesions, bone marrow, and lymph nodes across five provinces in Iran. DNA was extracted from the samples, and the nested PCR-amplified fragments were differentiated with agarose gel electrophoresis. The nested PCR assay successfully identified Leishmania major, Leishmania tropica, and Leishmania infantum with high accuracy. Among 156 microscopy-positive samples, L. major was detected in 84 cases, L. tropica was detected in 64 cases, and L. infantum was detected in 8 cases. The results obtained were fully consistent with those from a commercial real-time PCR diagnostic kit. Phylogenetic analysis supported the differentiation of Leishmania species. However, among 33 suspected cases, 14 samples were negative by all three methods (microscopy, commercial PCR kit, and nested PCR), 7 samples tested positive by both molecular methods, 8 samples were positive only with the commercial PCR kit, and 4 samples were positive exclusively by nested PCR. The findings indicate that the nested PCR assay targeting size polymorphisms in the rDNA region is a cost-effective method for detection and identification of Leishmania species in clinical specimens, particularly when microscopy results are inconclusive.
{"title":"Detection and Identification of Leishmania major, Leishmania tropica, and Leishmania infantum in Clinical Samples Based on Size Polymorphism of Partially Amplified Ribosomal DNA.","authors":"Reza Mohammadi Manesh, Somayeh Mousavi, Parisa Mousavi, Azadeh Zolfaghari, Zabihollah Zarei, Iraj Sharifi, Hossein Zarrinfar, Seyed Hossein Hejazi, Behrooz Ataei, Mehdi Mohebali, Hossein Mirhendi","doi":"10.4269/ajtmh.24-0843","DOIUrl":"10.4269/ajtmh.24-0843","url":null,"abstract":"<p><p>Accurate Leishmania species identification is crucial for epidemiological aspects and disease management. This study aimed to detect and identify the main causative species of human cutaneous and visceral leishmaniasis in Iran using nested polymerase chain reaction (PCR) based on size polymorphism of the ribosomal DNA (rDNA) intergenic region. In total, 180 clinical samples, including 156 confirmed positive cases, 24 confirmed negative cases, and 33 suspected cases that tested negative by microscopy, were collected from skin lesions, bone marrow, and lymph nodes across five provinces in Iran. DNA was extracted from the samples, and the nested PCR-amplified fragments were differentiated with agarose gel electrophoresis. The nested PCR assay successfully identified Leishmania major, Leishmania tropica, and Leishmania infantum with high accuracy. Among 156 microscopy-positive samples, L. major was detected in 84 cases, L. tropica was detected in 64 cases, and L. infantum was detected in 8 cases. The results obtained were fully consistent with those from a commercial real-time PCR diagnostic kit. Phylogenetic analysis supported the differentiation of Leishmania species. However, among 33 suspected cases, 14 samples were negative by all three methods (microscopy, commercial PCR kit, and nested PCR), 7 samples tested positive by both molecular methods, 8 samples were positive only with the commercial PCR kit, and 4 samples were positive exclusively by nested PCR. The findings indicate that the nested PCR assay targeting size polymorphisms in the rDNA region is a cost-effective method for detection and identification of Leishmania species in clinical specimens, particularly when microscopy results are inconclusive.</p>","PeriodicalId":7752,"journal":{"name":"American Journal of Tropical Medicine and Hygiene","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676614/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145243412","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
James E Prusak, Sydney M Nemphos, Hannah C Green, Sallie L Fell, Cecily C Midkiff, Avelina Rodgers, Jillian Perret, Brooke Grasperge, Krystal Vail, Nana Minkah, Brandon Wilder, Berlin Londono-Renteria, Robert V Blair, Jennifer A Manuzak
The anatomical and immunological similarities between humans and nonhuman primates (NHPs) make NHPs a viable model for examining Plasmodium spp. infection outcomes. Plasmodium fragile was previously used to model human severe malaria in NHPs using rhesus macaques (RMs), but a thorough investigation of the clinical and pathological effects of RM P. fragile infection has not yet been conducted. In this study, we observed that experimental infection of a male RM with P. fragile-infected erythrocytes resulted in clinical signs of malaria, including anemia; changes in red and white blood cell distribution; changes in red blood cell morphology; and gross and histopathological alterations to vital organs, such as the liver, lungs, heart, and brain. Plasmodium fragile-infected red blood cells were also observed in the vasculature of major organs, including the spleen, liver, lung, and brain. These results suggest that experimental P. fragile infection of RMs is a translatable model of human malaria.
{"title":"Clinical and Pathological Outcomes of Experimental Plasmodium fragile Infection in a Rhesus Macaque.","authors":"James E Prusak, Sydney M Nemphos, Hannah C Green, Sallie L Fell, Cecily C Midkiff, Avelina Rodgers, Jillian Perret, Brooke Grasperge, Krystal Vail, Nana Minkah, Brandon Wilder, Berlin Londono-Renteria, Robert V Blair, Jennifer A Manuzak","doi":"10.4269/ajtmh.25-0222","DOIUrl":"10.4269/ajtmh.25-0222","url":null,"abstract":"<p><p>The anatomical and immunological similarities between humans and nonhuman primates (NHPs) make NHPs a viable model for examining Plasmodium spp. infection outcomes. Plasmodium fragile was previously used to model human severe malaria in NHPs using rhesus macaques (RMs), but a thorough investigation of the clinical and pathological effects of RM P. fragile infection has not yet been conducted. In this study, we observed that experimental infection of a male RM with P. fragile-infected erythrocytes resulted in clinical signs of malaria, including anemia; changes in red and white blood cell distribution; changes in red blood cell morphology; and gross and histopathological alterations to vital organs, such as the liver, lungs, heart, and brain. Plasmodium fragile-infected red blood cells were also observed in the vasculature of major organs, including the spleen, liver, lung, and brain. These results suggest that experimental P. fragile infection of RMs is a translatable model of human malaria.</p>","PeriodicalId":7752,"journal":{"name":"American Journal of Tropical Medicine and Hygiene","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12676641/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145243724","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}