Search

Your search keyword '"Sadaow, Lakkhana"' showing total 185 results
Start Over Author "Sadaow, Lakkhana" Publication Year Range Last 10 years
185 results on '"Sadaow, Lakkhana"'

11. Improved diagnostic sensitivity of human strongyloidiasis using point-of-care mixed recombinant antigen-based immunochromatography

Author

Boonroumkaew Patcharaporn, Sadaow Lakkhana, Janwan Penchom, Rodpai Rutchanee, Sanpool Oranuch, Buadee Punyisa, Suprom Chanida, Thanchomnang Tongjit, Intapan Pewpan M., and Maleewong Wanchai

Subjects
strongyloidiasis, neglected tropical disease, recombinant antigen, point-of-care, serodiagnosis, immunochromatography test, Infectious and parasitic diseases, RC109-216
Abstract

Strongyloidiasis is a neglected tropical disease that can cause fatal complications due to hyperinfection and disseminated strongyloidiasis in immunocompromised patients. We used two Strongyloides stercoralis recombinant antigenic proteins, L3NieAg.01 (NIE) and IgG-immunoreactive antigen (SsIR), to develop the recombinant antigen-based immunochromatography test (ICT) kit. We constructed and compared kits using either the NIE (NIE ICT kit) or the SsIR (SsIR ICT kit) antigens and a kit using a mixture of both (NIE-SsIR ICT kit) for detection of anti-Strongyloides IgG antibody in human serum samples. Serum samples from normal healthy individuals (Group I, n = 40), proven strongyloidiasis patients (Group II, n = 100), and those with other parasitic infections (Group III, n = 154) were evaluated. Sensitivity and specificity were 81.0% and 84.0% for the NIE ICT kit, 89.0% and 83.5% for the SsIR ICT kit, and 95.0% and 90.2% for the NIE-SsIR ICT kit, respectively. The NIE-SsIR ICT kit provided the best diagnostic results; it can supplement stool examination for clinical diagnosis and can be used to screen for asymptomatic S. stercoralis infection in people at risk in endemic areas. The NIE-SsIR ICT kit can also be used in large-scale sero-epidemiological investigations in endemic areas without the need for additional facilities or ancillary supplies.

Published
2023
Full Text
View/download PDF

16. Bacterial community structure of Anopheles hyrcanus group, Anopheles nivipes, Anopheles philippinensis, and Anopheles vagus from a malaria-endemic area in Thailand

Author

Boonroumkaew, Patcharaporn, primary, Rodpai, Rutchanee, additional, Saeung, Atiporn, additional, Aupalee, Kittipat, additional, Saingamsook, Jassada, additional, Poolphol, Petchaboon, additional, Sadaow, Lakkhana, additional, Sanpool, Oranuch, additional, Janwan, Penchom, additional, Thanchomnang, Tongjit, additional, Intapan, Pewpan M., additional, and Maleewong, Wanchai, additional

Published
2023
Full Text
View/download PDF

21. Prevalence of intestinal parasitic infections and genetic differentiation of Strongyloides stercoralis among migrant workers from Myanmar, Lao PDR and Cambodia in northeastern Thailand

Author

Sangwalee, Wararat, primary, Norkaew, Jun, additional, Inthachak, Sengchoy, additional, Janwan, Penchom, additional, Rodpai, Rutchanee, additional, Sanpool, Oranuch, additional, Sadaow, Lakkhana, additional, Boonroumkaew, Patcharaporn, additional, Intapan, Pewpan M., additional, Maleewong, Wanchai, additional, and Thanchomnang, Tongjit, additional

Published
2022
Full Text
View/download PDF

23. Evaluation of total immunoglobulin G and subclass antibodies in an enzyme-linked immunosorbent assay for serodiagnosis of human amebic liver abscess

Author

Janwan, Penchom, primary, Sadaow, Lakkhana, additional, Rodpai, Rutchanee, additional, Yamasaki, Hiroshi, additional, Luvira, Vor, additional, Sukeepaisarnjaroen, Wattana, additional, Kitkhuandee, Amnat, additional, Paonariang, Krisada, additional, Sanpool, Oranuch, additional, Boonroumkaew, Patcharaporn, additional, Thanchomnang, Tongjit, additional, Mita, Toshihiro, additional, Intapan, Pewpan M., additional, and Maleewong, Wanchai, additional

Published
2022
Full Text
View/download PDF

24. First molecular identification and report of genetic diversity of Strongyloides stercoralis, a current major soil-transmitted helminth in humans from Lao People’s Democratic Republic

Author

Laymanivong, Sakhone, Hangvanthong, Bouasy, Insisiengmay, Bounnaloth, Vanisaveth, Viengxay, Laxachack, Pinnakhone, Jongthawin, Jurairat, Sanpool, Oranuch, Thanchomnang, Tongjit, Sadaow, Lakkhana, Phosuk, Issarapong, Rodpai, Rutchanee, Maleewong, Wanchai, and Intapan, Pewpan M.

Published
2016
Full Text
View/download PDF

26. High Prevalence of Intestinal Capillariasis in Chronic Diarrhea Patients in Thailand: Serological Screening Using a Rapid Lateral-Flow Immunochromatographic Assay

Author

Prasongdee, Thidarat K., primary, Seesui, Krongkaew, additional, Sadee, Phuangphaka, additional, Sadaow, Lakkhana, additional, Sukeepaisarnjaroen, Wattana, additional, Kraiklang, Ratthaphol, additional, Sanpool, Oranuch, additional, Maleewong, Wanchai, additional, and Intapan, Pewpan M., additional

Published
2022
Full Text
View/download PDF

28. Evaluation of total immunoglobulin G and subclass antibodies in an enzymelinked immunosorbent assay for serodiagnosis of human amebic liver abscess.

Author

Janwan, Penchom, Sadaow, Lakkhana, Rodpai, Rutchanee, Hiroshi Yamasaki, Luvira, Vor, Sukeepaisarnjaroen, Wattana, Kitkhuandee, Amnat, Paonariang, Krisada, Sanpool, Oranuch, Boonroumkaew, Patcharaporn, Thanchomnang, Tongjit, Toshihiro Mita, Intapan, Pewpan M., and Wanchai Maleewong

Subjects
LIVER abscesses, IMMUNOGLOBULIN G, SERODIAGNOSIS, IMMUNOGLOBULINS, ENZYME-linked immunosorbent assay, ENTAMOEBA histolytica, PARASITIC diseases
Abstract

Background. Amebic liver abscess (ALA) caused by Entamoeba histolytica is usually diagnosed based on its clinical symptoms, medical imaging abnormalities of the liver, and serological tests, the most common being the enzyme-linked immunosorbent assay (ELISA). For more than three decades, no investigation has evaluated the diagnostic performance of immunoglobulin G (IgG) subclasses in the serodiagnosis of ALA. Herein, we assessed the efficiencies of anti-amebic IgG and IgG subclasses for diagnosing ALA. Methods. A serological ELISA-based test was performed to assess its diagnostic performance using a total of 330 serum samples from ALA patients (nD14), healthy individuals (nD40), and patients with other diseases (nD276). Results. ELISA targeting the total IgG antibody to E. histolytica antigen exhibited 100% sensitivity 95% CI [76.8-100.0] and 97.8% specificity 95% CI [95.5-99.1], whereas the assay targeting IgG1 showed the same sensitivity (100% 95% CI [76.8-100.0]) and a slightly higher specificity (99.1% 95% CI [97.3-99.8]). The other IgG subclasses (IgG2, IgG3, and IgG4) displayed a lower sensitivity and specificity. The sensitivity and specificity did not significantly differ between tests measuring total IgG and IgG1 (Exact McNemar's test; p > 0.05), with a concordance of 98.2%, represented by a Cohen's kappa of 0.83 (p < 0.001), indicating almost perfect agreement. Conclusion. ELISA targeting IgG1 can provide valuable information to clinicians in differentiating ALA from other parasitic diseases, cancers, cirrhosis, and viral hepatitis. However, enzyme-conjugated anti-human total IgG is cheaper than anti-human IgG subclasses. Therefore, we suggest that total IgG-based ELISA is sufficient for the routine serodiagnosis of human ALA and possibly other clinical manifestations of invasive amebiasis. [ABSTRACT FROM AUTHOR]

Published
2022
Full Text
View/download PDF

29. Exposure to dexamethasone modifies transcriptomic responses of free-living stages of Strongyloides stercoralis

Author

Rodpai, Rutchanee, primary, Sanpool, Oranuch, additional, Thanchomnang, Tongjit, additional, Laoraksawong, Pokkamol, additional, Sadaow, Lakkhana, additional, Boonroumkaew, Patcharaporn, additional, Wangwiwatsin, Arporn, additional, Wongkham, Chaisiri, additional, Laummaunwai, Porntip, additional, Ittiprasert, Wannaporn, additional, Brindley, Paul J., additional, Intapan, Pewpan M., additional, and Maleewong, Wanchai, additional

Published
2021
Full Text
View/download PDF

31. Development of Immunochromatographic Test Kit for Rapid Detection of Specific IgG4 Antibody in Whole-Blood Samples for Diagnosis of Human Gnathostomiasis

Author

Janwan, Penchom, primary, Intapan, Pewpan M., additional, Sadaow, Lakkhana, additional, Rodpai, Rutchanee, additional, Yamasaki, Hiroshi, additional, Boonroumkaew, Patcharaporn, additional, Sanpool, Oranuch, additional, Thanchomnang, Tongjit, additional, Sadee, Phuangphaka, additional, and Maleewong, Wanchai, additional

Published
2021
Full Text
View/download PDF

32. High prevalence of opisthorchiasis in rural populations from Khammouane Province, central Lao PDR: serological screening using total IgG- and IgG4-based ELISA

Author

Phupiewkham, Weeraya, primary, Rodpai, Rutchanee, additional, Inthavongsack, Somchith, additional, Laymanivong, Sakhone, additional, Thanchomnang, Tongjit, additional, Sadaow, Lakkhana, additional, Boonroumkaew, Patcharaporn, additional, Sanpool, Oranuch, additional, Janwan, Penchom, additional, Intapan, Pewpan M, additional, and Maleewong, Wanchai, additional

Published
2021
Full Text
View/download PDF

34. Effectiveness of Strongyloides Recombinant IgG Immunoreactive Antigen in Detecting IgG and IgG4 Subclass Antibodies for Diagnosis of Human Strongyloidiasis Using Rapid Immunochromatographic Tests

Author

Boonroumkaew, Patcharaporn, primary, Sadaow, Lakkhana, additional, Sanpool, Oranuch, additional, Rodpai, Rutchanee, additional, Thanchomnang, Tongjit, additional, Phupiewkham, Weeraya, additional, Intapan, Pewpan M., additional, and Maleewong, Wanchai, additional

Published
2020
Full Text
View/download PDF

37. Development and Accuracy Evaluation of Lateral Flow Immunoassay for Rapid Diagnosis of Schistosomiasis Mekongi in Humans.

Author

Rodpai, Rutchanee, Sadaow, Lakkhana, Sanpool, Oranuch, Boonroumkaew, Patcharaporn, Thanchomnang, Tongjit, Laymanivong, Sakhone, Janwan, Penchom, Limpanont, Yanin, Chusongsang, Phiraphol, Ohmae, Hiroshi, Yamasaki, Hiroshi, Lv, Zhiyue, Intapan, Pewpan M., and Maleewong, Wanchai

Subjects
*SCHISTOSOMIASIS, *IMMUNOASSAY, *ENDEMIC diseases, *DIAGNOSIS, *DISEASE prevalence, *TRICHINOSIS
Abstract

Schistosoma mekongi infection is endemic in countries along the Mekong River and certain of its tributaries in the lower Mekong basin, especially in Lao People's Democratic Republic and Cambodia. Diagnosis of schistosomiasis is crucial before treatment and epidemiological surveys before and/or after an intervention, such as a mass drug administration. A newly developed immunochromatographic test (ICT) for the diagnosis of schistosomiasis mekongi, based on antiparasite antibody detection in human sera, was evaluated. The schistosomiasis mekongi-ICT (Smk-ICT) strip was developed using somatic antigen from adult S. mekongi. In total, 209 serum samples were examined, including 14 from parasitologically proven schistosomiasis mekongi patients, 30 from schistosomiasis japonica patients, other parasitosis (n = 135), and healthy volunteers (n = 30) from areas not endemic for S. mekongi. Eleven schistosomiasis mekongi samples were positive according to the Smk-ICT, whereas all healthy control samples were negative. Cross-reactions with paragonimiasis heterotremus, sparganosis, trichinellosis, and taeniasis saginata samples were observed at 2.4% (4/165). The diagnostic sensitivity, specificity, positive predictive value, negative predictive value, and accuracy were 78.6% (95% confidence interval [CI] 49.2–95.3), 97.6% (95% CI 93.9–99.3), 73.3% (95% CI 44.9–92.2), 98.2% (95% CI 94.7–99.6), and 96.1% (95% CI 92.1–98.4), respectively. The Smk-ICT kit might be useful to assess the prevalence of disease before establishing transmission control and mass deworming campaigns in countries in the Mekong River subregion. [ABSTRACT FROM AUTHOR]

Published
2022
Full Text
View/download PDF

42. Molecular Identification of Trichuris suis and Trichuris trichiura Eggs in Human Populations from Thailand, Lao PDR, and Myanmar

Author

Phosuk, Issarapong, primary, Rodpai, Rutchanee, additional, Janwan, Penchom, additional, Thanchomnang, Tongjit, additional, Intapan, Pewpan M., additional, Laymanivong, Sakhone, additional, Pa Aung, Win Pa, additional, Anamnart, Witthaya, additional, Sanpool, Oranuch, additional, Wijit, Adulsak, additional, Maleewong, Wanchai, additional, and Sadaow, Lakkhana, additional

Published
2018
Full Text
View/download PDF

45. First report and molecular identification of Opisthorchis viverrini infection in human communities from Lower Myanmar

Author

Aung, Win Pa Pa, primary, Htoon, Thi Thi, additional, Tin, Htay Htay, additional, Thinn, Kyi Kyi, additional, Sanpool, Oranuch, additional, Jongthawin, Jurairat, additional, Sadaow, Lakkhana, additional, Phosuk, Issarapong, additional, Rodpai, Rutchanee, additional, Intapan, Pewpan M., additional, and Maleewong, Wanchai, additional

Published
2017
Full Text
View/download PDF

48. Development of an immunochromatographic device to detect antibodies for rapid diagnosis of human angiostrongyliasis.

Author

Somboonpatarakun, Chalermchai, Intapan, Pewpan M., Sadaow, Lakkhana, Rodpai, Rutchanee, Sanpool, Oranuch, and Maleewong, Wanchai

Subjects
CENTRAL nervous system diseases, ANGIOSTRONGYLUS cantonensis, ENZYME-linked immunosorbent assay, CLINICAL pathology, DIAGNOSTIC equipment, IMMUNOGLOBULINS, VIRAL antibodies, EOSINOPHILIC granuloma
Abstract

Cerebral angiostrongyliasis is a central nervous system disease caused by Angiostrongylus cantonensis and can produce eosinophilic meningitis or meningoencephalitis in humans. Sero-immunological techniques, such as the enzyme-linked immunosorbent assay (ELISA) and immunoblotting, are most commonly used for the diagnosis of human angiostrongyliasis. However, diagnosis in remote areas remains problematic because sophisticated equipment and specialized skills are required. To overcome, we have developed the immunochromatographic test (ICT) kit for rapid serological diagnosis of angiostrongyliasis through the detection of anti- A. cantonensis -specific antibodies in human serum. A recombinant A. cantonensis galectin-2 (rAcGal2) from young adult female worms was used as an antigen for the ICT kit development. Diagnostic values were evaluated and compared using the ELISA. The sensitivity, specificity and positive and negative predictive values of the ICT kit were 87.0, 96.5, 94.6 and 91.4%, respectively, and those of the ELISA were 91.0, 97.2, 95.8 and 94.0%, respectively. The concordance of the ICT kit was 93.9%. We, thus, determined that the ICT kit is sensitive and specific and provides reliable diagnostic results. It is rapid and simple to perform and can be utilized for both point-of-care diagnosis in the bedside laboratory and epidemiological surveys in endemic regions where access to diagnostic equipment is limited. [ABSTRACT FROM AUTHOR]

Published
2020
Full Text
View/download PDF

49. An immunochromatographic test using whole blood for rapid diagnosis of human paragonimiasis and its diagnostic usefulness

Author

Boonroumkaew, Patcharaporn, Sadaow, Lakkhana, Janwan, Penchom, Rodpai, Rutchanee, Sanpool, Oranuch, Thanchomnang, Tongjit, Yamasaki, Hiroshi, Intapan, Pewpan M., and Maleewong, Wanchai

Abstract

Paragonimiasis is a harmful food-borne zoonosis caused by lung flukes of the genus Paragonimus. The disease is found on most continents, several million people are at risk of infection, and it is a re-emerging disease in developing countries. The gold standard for diagnosis of pulmonary paragonimiasis requires the finding of eggs in sputa and/or fecal samples. In ectopic paragonimiasis cases, eggs are typically not seen, and supportive information is required such as a history of eating freshwater crabs or crayfishes, radiographic findings and immunological tests. Here, we developed a proof of concept based on lateral flow assay, an immunochromatographic test kit, named the paragonimiasis whole-blood test kit, for detection of specific IgG antibody in simulated whole-blood samples (WBSs) using worm excretory-secretory antigens to diagnose human paragonimiasis. The laboratory diagnostic values of this kit were compared with the detected IgG in serum samples. In simulated WBSs, the diagnostic sensitivity and specificity were 97.8 % and 96.1 %, respectively, while for serum samples, these values were 100.0 % and 94.8 %, respectively. The comparative IgG antibody detections whether a result was positive or negative between simulated WBSs and serum samples did not differ significantly with a concordance of 97.8 % in laboratory conditions using a circumscribed set of samples. The tool is fast and easy to use. The next step involves observing and evaluating native whole blood samples and using specific recombinant antigens need to be evaluated for support diagnosis of paragonimiasis caused by P. heterotremus, P. westermaniand P. miyazakiiat the bedside or at local and remote hospitals with limited facilities. It will also be valuable for epidemiological surveys in Asia where paragonimiasis is endemic.

Published
2024
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results