Anti-phenolic glycolipid-I seropositivity among household contacts of leprosy patients in Egypt

被引:0
|
作者
Salah, Eman Mohamed [1 ]
Khalil, Haidy [2 ,3 ]
Moussa, Mai Ebrahim [1 ]
Shalaby, Rasha E. [4 ,5 ]
Diab, Heba Mahmoud [6 ]
机构
[1] Helwan Univ, Fac Med, Dept Dermatol Androl Sexual Med & STDs, Cairo, Egypt
[2] Benha Natl Univ, Fac Med, Dept Microbiol & Immunol, Obour City, Egypt
[3] Helwan Univ, Fac Med, Dept Microbiol & Immunol, Cairo, Egypt
[4] Tanta Univ, Fac Med, Dept Microbiol & Immunol, Tanta, Egypt
[5] Galala Univ, Fac Med, Dept Basic Med Sci, Galala City, Suez, Egypt
[6] Ain Shams Univ, Fac Med, Dept Dermatol Venereol & Androl, Cairo, Egypt
关键词
Leprosy; Household contacts; Biomarker; Anti-PGL-I antibodies; ELISA;
D O I
10.1007/s00403-024-03462-7
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Leprosy is a chronic, debilitating disease lacking a definitive diagnostic biomarker. Serum anti-phenolic glycolipid-I (PGL-I) IgM antibody level is considered an important diagnostic and prognostic marker for leprosy patients. However, there is limited evidence on the role of anti-PGL-I IgM antibody level as early predictive biomarker of subclinical infection among Egyptian household contacts of leprosy patients. This study investigates the relationship between specific leprosy risk factors, diagnostic parameters of eighty-three leprosy cases, and serum anti-PGL-I IgM antibody levels in their corresponding household contacts. Our results demonstrate that anti-PGL-I IgM antibody level was significantly higher among contacts when more than four residents shared the same room with a leprosy case (p = 0.032). Additionally, anti-PGL-I IgM antibody level markedly increased in contacts of leprosy cases with disabilities (p = 0.001) or damaged nerves (p = 0.001). Our ROC curve analysis of anti-PGL-I antibody level as a predictor of exposure or infection among contacts revealed a cut-off value of 0.1, with a sensitivity of 75.0% and a specificity of 54.5%, indicating that most exposed household contacts are correctly identified. The overall accuracy of the ROC curve analysis was 72.3%, highlighting the practical utility of anti-PGL-I antibody level as a predictor for exposure or infection among household leprosy contacts. In conclusion, seropositivity of anti-PGL-I antibodies (> 0.1) among household leprosy contacts may be associated with a higher leprosy exposure risk. Continuous monitoring of anti-PGL-I antibody level in household leprosy contacts may potentially contribute to early detection and management of leprosy.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] Risk-benefit assessment of Bacillus Calmette-Guerin vaccination, anti-phenolic glycolipid I serology, and Mitsuda test response: 10-year follow-up of household contacts of leprosy patients
    Araujo, Sergio
    Figueiredo Rezende, Marina Monteiro
    Rodrigues de Sousa, Diogo Carrijo
    Rosa, Marasa Resende
    dos Santos, Danielle Cristina
    Goulart, Luiz Ricardo
    Bernardes Goulart, Isabela Maria
    REVISTA DA SOCIEDADE BRASILEIRA DE MEDICINA TROPICAL, 2015, 48 (06) : 739 - 745
  • [22] Bacilloscopy and polymerase chain reaction of slit-skin smears and anti-phenolic glycolipid-I serology for Hansen's disease diagnosis
    Lima, Filipe Rocha
    de Paula, Natalia Aparecida
    Simoes, Mateus Mendonca Ramos
    Manso, Gabriel Martins da Costa
    Albertino, Gustavo Sartori
    Felisbino, Giovani Cesar
    Antunes, Vanderson Mayron Granemann
    Perecin, Fernanda Andre Martins Cruz
    Westin, Andrezza Telles
    Lugao, Helena Barbosa
    Frade, Marco Andrey Cipriani
    FRONTIERS IN MEDICINE, 2022, 9
  • [23] The relation between seroprevalence of antibodies against phenolic glycolipid-I among school children and leprosy endemicity in Brazil
    Buhrer-Sekula, Samira
    van Beers, Stella
    Oskam, Linda
    Lecco, Rita
    Madeira, Elisabete Santos
    Lopes Dutra, Marco Antonio
    Luis, Magali Chaves
    Faber, William R.
    Klatser, Paul R.
    REVISTA DA SOCIEDADE BRASILEIRA DE MEDICINA TROPICAL, 2008, 41 : 81 - 88
  • [24] IgM anti-phenolic glycolipid-I antibody measurements from skin-smear sites: Correlation with venous antibody levels and the bacterial index
    Butlin, CR
    Soares, D
    Neupane, KD
    Failbus, SS
    Roche, PW
    INTERNATIONAL JOURNAL OF LEPROSY AND OTHER MYCOBACTERIAL DISEASES, 1997, 65 (04) : 465 - 468
  • [25] IGM SERUM ANTIBODIES TO PHENOLIC GLYCOLIPID-I AND CLINICAL LEPROSY - 2 YEARS OBSERVATION IN A COMMUNITY WITH HYPERENDEMIC LEPROSY
    BAGSHAWE, AF
    GARSIA, RJ
    BAUMGART, K
    ASTBURY, L
    INTERNATIONAL JOURNAL OF LEPROSY AND OTHER MYCOBACTERIAL DISEASES, 1990, 58 (01) : 25 - 30
  • [26] SEROLOGICAL SPECIFICITY OF PHENOLIC GLYCOLIPID-I FROM MYCOBACTERIUM-LEPRAE AND USE OF SERODIAGNOSIS IN LEPROSY
    CHO, SN
    YANAGIHARA, DL
    HUNTER, SW
    GELBER, RH
    BRENNAN, PJ
    INTERNATIONAL JOURNAL OF LEPROSY AND OTHER MYCOBACTERIAL DISEASES, 1983, 51 (04) : 659 - 660
  • [27] SEROLOGICAL SPECIFICITY OF PHENOLIC GLYCOLIPID-I FROM MYCOBACTERIUM-LEPRAE AND USE IN SERODIAGNOSIS OF LEPROSY
    CHO, SN
    YANAGIHARA, DL
    HUNTER, SW
    GELBER, RH
    BRENNAN, PJ
    INFECTION AND IMMUNITY, 1983, 41 (03) : 1077 - 1083
  • [28] SEQUENTIAL MONITORING OF LEPROSY PATIENTS WITH SERUM ANTIBODY-LEVELS TO PHENOLIC GLYCOPIPID-I, A SYNTHETIC ANALOG OF PHENOLIC GLYCOLIPID-I, AND MYCOBACTERIAL LIPOARABINOMANNAN
    MEEKER, HC
    SCHULLERLEVIS, G
    FUSCO, F
    GIARDINABECKET, MA
    SERSEN, E
    LEVIS, WR
    INTERNATIONAL JOURNAL OF LEPROSY AND OTHER MYCOBACTERIAL DISEASES, 1990, 58 (03) : 503 - 511
  • [29] SERUM IGA1 AND IGM ANTIBODIES AGAINST MYCOBACTERIUM-LEPRAE-DERIVED PHENOLIC GLYCOLIPID-I - A COMPARATIVE-STUDY IN LEPROSY PATIENTS AND THEIR CONTACTS
    CHUJOR, CSN
    BERNHEIMER, H
    LEVIS, WR
    SCHWERER, B
    INTERNATIONAL JOURNAL OF LEPROSY AND OTHER MYCOBACTERIAL DISEASES, 1991, 59 (03) : 441 - 449
  • [30] IGA ANTIBODIES AGAINST PHENOLIC GLYCOLIPID-I FROM MYCOBACTERIUM-LEPRAE IN SERUM OF LEPROSY PATIENTS AND CONTACTS - SUBCLASS DISTRIBUTION AND RELATION TO DISEASE-ACTIVITY
    SCHWERER, B
    CHUJOR, CSN
    BERNHEIMER, H
    RADL, J
    HAAIJMAN, JJ
    MEEKER, HC
    SERSEN, G
    LEVIS, WR
    CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1989, 53 (02): : 202 - 211