Urquiza Mauricio, Sánchez Ricardo, Amaya Jairo, León Sandra, Acosta Jenny, Patarroyo Manuel A, Camargo Milena, Patarroyo Manuel E
Virology, Fundacion Instituto de Inmunologia de Colombia, Carrera 50, #26-00, Bogota 020304, Colombia.
J Clin Microbiol. 2008 Nov;46(11):3714-20. doi: 10.1128/JCM.00551-08. Epub 2008 Sep 17.
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.
一种用于检测有患宫颈癌风险女性人乳头瘤病毒(HPV)感染的血清学检测方法,可基于保守的L1肽段,这些肽段具有低水平的抗原性,能被感染高危HPV(HR-HPV)型别且患有宫颈病变的患者体内抗体特异性识别。目的是评估L1肽段18283、18294和18301与病毒样颗粒(VLP)在识别女性这些感染方面的能力。共对391名感染HPV的女性志愿者进行了访谈,并采集外周血和宫颈细胞用于检测抗HPV抗体和HPV DNA;所有患者均进行了巴氏涂片检查;根据妇科标准,287名患者被转诊进行阴道镜检查或活检。通过使用林氏系数(rho值)确定的一致性水平表明,75%至83%的HR-HPV DNA阳性宫颈病变女性体内有能识别VLP和肽段18283、18294或18301的抗体,而15%至23%细胞学正常的HPV DNA阴性女性体内有能识别这三种肽段的抗体,45%有能识别VLP的抗体。对于HPV DNA阳性宫颈病变患者,肽段与VLP在抗体检测方面的一致性率更高。肽段18283、18294和18301在检测HR-HPV DNA阳性宫颈病变方面显示出相似的敏感性,且比VLP更具特异性。肽段18301可能在检测意义不明确的非典型鳞状细胞的HPV DNA阴性女性体内的保护性抗体。这些肽段可用于设计一种血清学检测方法,以检测患有宫颈病变且有患宫颈癌风险的女性中的HR-HPV感染。