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Specificity of L1 Peptides versus Virus-Like Particles for Detection of Human Papillomavirus-Positive Cervical Lesions in Females Attending Engativa Hospital, Bogota, Colombia▿

机译:在哥伦比亚波哥大Engativa医院就诊的女性中,检测人乳头瘤病毒阳性宫颈病变的L1肽对病毒样颗粒的特异性▿

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摘要

A serological test for the detection of human papillomavirus (HPV) infection in females at risk of developing cervical cancer could be based on conserved L1 peptides with low levels of antigenicity specifically recognized by antibodies from patients with cervical lesions infected with high-risk HPV (HR-HPV) types. The aim was to assess the ability of L1 peptides 18283, 18294, and 18301 compared with the ability of virus-like particles (VLPs) to identify these infections in females. A total of 391 HPV-infected female volunteers were interviewed, and peripheral blood and cervical cells were obtained for detection of anti-HPV antibodies and HPV DNA; all of the patients had a Pap smear test; 287 patients were referred for colposcopy or biopsy, according to gynecological criteria. The level of agreement, as determined by the use of the Lin coefficient (rho value), showed that 75 to 83% of females with HR-HPV DNA-positive cervical lesions had antibodies that recognized VLPs and peptide 18283, 18294, or 18301, while 15 to 23% of the HPV DNA-negative females with a normal cytology had antibodies that recognized these three peptides and 45% had antibodies that recognized VLPs. The rate of agreement between peptides and VLPs for antibody detection was higher for patients with HPV DNA-positive cervical lesions. Peptides 18283, 18294, and 18301 showed similar sensitivities for the detection of HR-HPV DNA-positive cervical lesions and were more specific than VLPs. Peptide 18301 might be detecting protective antibodies in HPV DNA-negative females with atypical squamous cells of undetermined significance. These peptides could be useful for the design of a serology test for the detection of HR-HPV infection in females with cervical lesions and at risk of cervical cancer.
机译:用于检测有宫颈癌风险的女性中人乳头瘤病毒(HPV)感染的血清学检测可以基于具有低抗原性水平的保守L1肽,这些肽被高风险HPV感染的宫颈病变患者的抗体特异性识别-HPV)类型。目的是评估L1肽18283、18294和18301的能力与病毒样颗粒(VLP)识别女性感染的能力相比。总共对391名被HPV感染的女性志愿者进行了采访,并获得了外周血和宫颈细胞以检测抗HPV抗体和HPV DNA。所有患者均进行了子宫颈抹片检查;根据妇科标准,将287例患者转诊接受阴道镜检查或活检。通过使用Lin系数(rho值)确定的一致程度表明,HR-HPV DNA阳性宫颈病变的女性中有75%至83%的女性具有识别VLP和18283、18294或18301肽的抗体,细胞学检查正常的HPV DNA阴性女性中,有15%至23%的抗体具有识别这三种肽的抗体,而有45%的女性具有识别VLP的抗体。 HPV DNA阳性宫颈病变患者的肽和VLP之间用于抗体检测的一致性更高。肽18283、18294和18301对HR-HPV DNA阳性子宫颈病变的检测显示出相似的灵敏度,并且比VLP更具特异性。多肽18301可能正在检测HPV DNA阴性的女性,具有非典型意义的非典型鳞状细胞中的保护性抗体。这些肽可用于设计血清学测试,以检测患有宫颈病变和有宫颈癌风险的女性的HR-HPV感染。

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