Summary:Particular human papillomavirus (HPV) subtypes are implicated in the genesis of abnormal cervical cytology and cervical cancer. While most immunocompetent hosts clear HPV infection with no sequelae, some develop premalignant cytological changes of whom a minority subsequently progress to overt carcinoma. Immunocompromised patients, such as renal allograft recipients and HIV-infected individuals, have a higher rate of cytological abnormalities. This is thought to be due to prolonged persistence of virus due to impaired clearance by the immune system. We undertook a retrospective review of the cervical cytology of all women who underwent BMT at two transplant centres and who had cervical smears performed between 1990 and 1998. The rate of cytological abnormalities was significantly higher than in the general population before BMT (ageadjusted odds ratio (OR) 2.2, P = 0.02) and after BMT (OR 7.0, P Ͻ 0.0001). After BMT, allogeneic recipients had a higher rate of abnormalities than did autologous patients (OR 2.6, P = 0.02) although only allogeneic recipients had a higher rate of abnormalities post-BMT compared to pre-BMT (allogeneic OR 6.8, P = 0.004). These observations suggest that pre-transplant disease and treatment factors increase the risk of cytologic abnormalities and that transplant-related factors such as conditioning therapy and immunosuppression further increase this risk. These data suggest that more frequent screening may be required in these at-risk groups, especially allogeneic recipients. Prospective studies are required to further evaluate cytological abnormalities and HPV shedding in these populations. infection by DNA hybridisation, 1 some studies have reported rates of up to 46% in at-risk populations when evaluated by very sensitive tests such as polymerase chain reaction (PCR). 2 HPV consists of over 80 genotypes with various subtypes showing differential tissue tropism and having associations with specific disease manifestations. Current evidence now strongly implicates HPV as a causative agent in cervical cancer, including epidemiological data from large casecontrol studies and the demonstration of HPV genomes in 93% of invasive cervical cancers. Two 'high risk' types, HPV-16 and HPV-18, are found in 40-60% and 10-20% of invasive cancers, respectively. [3][4][5][6] The highest prevalence of HPV-induced cervical cytological changes occurs in the early part of the third decade, 7 while the mean age of invasive carcinoma occurs in the middle of the sixth decade, 8 suggesting a prolonged latent phase of infection before the onset of overt malignant disease. This forms the basis of regular cytological screening, most commonly in the form of a Papanicolou (Pap) smear which detects cytological changes and allows intervention prior to the development of invasive disease.In the immunocompetent host, it has been demonstrated that infection is usually transient, with a reported median duration of 8 months. Seventy percent of women clear new infections within 12 months and 91% clear by 24 month...