Human papillomavirus genotypes in cervical cancer and vaccination challenges in Zimbabwe

被引:13
作者
Chin'ombe, Nyasha [1 ]
Sebata, Natasha L. [1 ]
Ruhanya, Vurayai [1 ]
Matarira, Hilda T. [2 ]
机构
[1] Univ Zimbabwe, Dept Med Microbiol, Harare, Zimbabwe
[2] Univ Zimbabwe, Dept Chem Pathol, Harare, Zimbabwe
关键词
PARTICLE VACCINE; HPV VACCINE; WOMEN; EFFICACY; TYPE-18; LESIONS; PERSISTENCE; PREVALENCE; INFECTION; BURDEN;
D O I
10.1186/1750-9378-9-16
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cervical cancer is one of the major causes of morbidity and mortality in women in Zimbabwe. This is mainly due to the high prevalence of high-risk human papillomavirus (HPV) genotypes in the population. So far, few studies have been done that showed the presence of high-risk genital HPV genotypes such as 16, 18, 31, 33, 52, 58 and 70 in Zimbabwean women with cervical cancer. The prevalence of HPV DNA in women with cervical cancer has been shown to range from 63% to 98%. The high-risk HPV 16, 18, 31, 33 and 58 were the most common genotypes in all the studies. The introduction of the new HPV vaccines, HPV2 and HPV4, which protect against HPV genotypes 16 and 18 into Zimbabwe is likely to go a long way in reducing deaths due to cervical cancer. However, there are few challenges to the introduction of the vaccines. The target population for HPV vaccination is at the moment not well-defined. The other challenge is that the current HPV vaccines confer only type-specific (HPV 16 and 18) immunity leaving a small proportion of Zimbabwean women unprotected against other high-risk HPV genotypes such as 31, 33 and 58. Future HPV vaccines such as the nanovalent vaccine will be more useful to Zimbabwe as they will protect women against more genotypes.
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页数:4
相关论文
共 44 条
[1]   Introducing HPV vaccine in developing countries - Key challenges and issues [J].
Agosti, Jan M. ;
Goldie, Sue J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (19) :1908-1910
[2]   The causal relation between human papillomavirus and cervical cancer [J].
Bosch, FX ;
Lorincz, A ;
Muñoz, N ;
Meijer, CJLM ;
Shah, KV .
JOURNAL OF CLINICAL PATHOLOGY, 2002, 55 (04) :244-265
[3]   Worldwide human papillomavirus etiology of cervical adenocarcinoma and its cofactors:: Implications for screening and prevention [J].
Castellsagué, X ;
Díaz, M ;
de Sanjosé, S ;
Muñoz, N ;
Herrero, R ;
Franceschi, S ;
Peeling, RW ;
Ashley, R ;
Smith, JS ;
Snijders, PJF ;
Meijer, CJLM ;
Bosch, FX .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (05) :303-315
[4]   Human papillomavirus genotypes in rural Mozambique [J].
Castellsagué, X ;
Menéndez, C ;
Loscertales, MP ;
Kornegay, JR ;
dos Santos, F ;
Gómez-Olivé, FX ;
Lloveras, B ;
Abarca, N ;
Vaz, N ;
Barreto, A ;
Bosch, FX ;
Alonso, P .
LANCET, 2001, 358 (9291) :1429-1430
[5]  
Chin'ombe N, 2000, PREVENTION CERVICAL
[6]  
Chirara M, 2001, Cent Afr J Med, V47, P32
[7]  
Chou P, 1991, Zhonghua Yi Xue Za Zhi (Taipei), V48, P81
[8]   Comparison of HPV type distribution in high-grade cervical lesions and cervical cancer: a meta-analysis [J].
Clifford, GM ;
Smith, JS ;
Aguado, T ;
Franceschi, S .
BRITISH JOURNAL OF CANCER, 2003, 89 (01) :101-105
[9]  
Desruisseau Andrew J, 2009, Infect Dis Obstet Gynecol, V2009, P810596, DOI 10.1155/2009/810596
[10]   Potential cost-effectiveness of the nonavalent human papillomavirus (HPV) vaccine [J].
Drolet, Melanie ;
Laprise, Jean-Francois ;
Boily, Marie-Claude ;
Franco, Eduardo L. ;
Brisson, Marc .
INTERNATIONAL JOURNAL OF CANCER, 2014, 134 (09) :2264-2268