Skip to main content

Is it time to shift the attention on early stages embryo development to avoid inconclusive evidence on HPV-related infertility: debate and proposal



Current evidence about in-vivo effects of HPV cannot definitively clarify the possible negative role of this worldwide common infection in early embryo development. However in-vitro evidence, seems to underline a possible negative effect of HPV in increasing blastocyst apoptosis and in reducing the endometrial implantation of trophoblastic cells. On these bases we believe that a new scientific approach is necessary to better understand the real role of male and female HPV infection in infertility and early pregnancy development.


English literature review of manuscripts focused on HPV infection and human reproduction was conducted. We performed a critical analysis of evidence and possible bias affecting both in-vivo and in-vitro studies regarding this topic.


The biggest limitation of the in-vivo studies is due to the inappropriate timing of HPV effects evaluation since evidence about in-vitro studies strongly suggests that a large part of HPV negative effects occurs during a very early stage of embryo development. All the efforts of the scientific community to investigate the real role of HPV in human reproduction disorders cannot underestimate the severe BIAS of actual evidence in postulating new hypothesis and research projects which are fundamental to clarify if HPV may be associated with unexplained couples infertility and early miscarriages.


If the relationship between HPV gametes infection and early human reproduction step impairment will be confirmed, the HPV male and couple vaccination may represent a reliable option to improve fertility in some couples affected by infertility actually classified as “idiopathic” but maybe linked to HPV infection.


Starting from our recent systematic literature review about “Male and Couple Fertility Impairment due to HPV-DNA Sperm Infection” we focused our attention on the controversies concerning HPV infection in human reproduction impairment [1]. Current evidence about in-vivo effects of HPV cannot definitively clarify the possible negative role of this worldwide common infection in early embryo development [26]. However, in-vitro evidence seems to underline a possible negative effect of HPV in increasing blastocyst apoptosis and in reducing the endometrial implantation of trophoblastic cells [715]. Despite Matovina et al. detected the HPV-DNA in miscarriages specimens without any significant association [16], in our knowledge only two clinical studies demonstrated a possible relationship between HPV and early pregnancy loss. Hermonat et al. comparing the prevalence of HPV in samples from spontaneous miscarriages and elective abortions found that 15 of the 25 spontaneous samples (60%) were positive for HPV-DNA sequences compared to only 3 of the 15 elective samples (20%) [2]. The higher percentage of HPV-DNA detection, if compared to voluntary abortions, lead the Authors to consider HPV as one of the possible etiologic agents responsible for early pregnancy loss. Perino et al., on a total of 199 couples undergoing to IVF cycles (in-vitro fertilization), found an increased risk of pregnancy loss both in case of male sperm infection (66.7% versus 15%) and of female cervical infection (40% versus 13.7%) [3].

Anyway the interesting results of Perino et al. should be interpreted with caution since several Authors reported approximately 24% of cervical HPV-DNA detection in women with ongoing pregnancy [17, 18].

Other 3 available studies (other than Matovina et al. [16]) failed to find a possible correlation between HPV infection and early miscarriages [46]. Skoczynski et al., on a total of 129 women, found the HPV-DNA in 17.7% of spontaneous miscarriages samples and in 24.4% of placenta from term deliveries [4]. Also Conde-Ferraez et al., comparing 127 women with spontaneous abortion attending for curettage and 127 pregnant women at-term, found an HPV cervical prevalence of 24.4% and 15.2% respectively without significant correlation between HPV infection and pregnancy loss [5]. Ticconi et al., analyzing retrospectively 49 cases of women with unexplained recurrent miscarriages and 475 healthy controls, found a cervical HPV prevalence of 26.53% in cases (13 of 49) and 61.89% in controls (294 of 475) confirming the absence of a causal association between HPV and miscarriages [6].


We believe that all the in-vivo studies conducted till now (except for the perspective one of Perino et al.) are affected by different BIAS which probably led to confusion in considering the final results. The first possible BIAS is related to the HPV types detected: all the cited studies focused in particular on high-risk (Hr) genotype 16 and 18 extending the search only to few other Hr-genotypes or low risk HPV 6/11. The second BIAS is related to the sample detection methods of HPV presence which did not permit to rule out the possible contaminations derived by the passage through the genital tract. Adjunctively the study by Conde-Ferraez et al. and Ticconi et al., focusing only on cervical HPV detection, did not consider the possible BIAS related to the viral clearance (at time of cervical sample the patients may have already cleared the virus) which can lead to an underestimation of the problem [19]. The third BIAS is related to the fact that all these studies are built without considering the new inputs provided by recent in-vitro evidence which demonstrated that HPV sperm infection seems to have a possible role in adverse blastocyst development [7, 14]. In particular it has been demonstrated that the spermatozoa is a vector for HPV transmission into fertilized oocytes and that the infected zygote (if the oocyte is fertilized) is able to perpetuate the viral genome expression at blastocyst stage and subsequently in trophoblastic cells [7, 13, 20].

On these bases we believe that a new scientific approach is necessary to better understand the real role of male and female HPV infection in early pregnancy development and infertility. We think that the recent in-vitro evidence on this field represents a good starting point to plan new perspective studies and to avoid the above mentioned BIAS.

Yet in 1996 Cabrera et al. in a murine experimental study demonstrated that spermatozoa carrying HPV-16 and −18 viral genome can be transfected into a mouse blastocyst with viral DNA localization both in the inner cells mass and trophoblastic cells [14]. The consequences of this possible “colonization” were subsequently evaluated by different Authors who confirmed the possible adverse effects of HPV at different steps of human embryo development. Calinisan et al. found that mouse blastocysts incubated with HPV-DNA-16 fragments showed an increased rate of DNA fragmentation and apoptosis [15]. This interesting result was subsequently confirmed and deepen by Henneberg et al. who defined the exact timing of HPV embryo impairment. In particular the Author showed how HPV-16 and −18 are able to inhibit the embryo development only at 2 cells stage (but not at 4–8 cells stage) with a peak percentage of about 30% after HPV-16 exposure and a major inhibition of blastocyst hatching process after HPV-18 exposure [10]. Different Authors demonstrated also the negative effect of HPV presence in trophoblastic cells which could result in abnormal placentation and maybe in early pregnancy loss. You et al. demonstrated that trophoblastic cells, like squamous epithelium, are broadly permissive for HPV showing some similarities in the gene expression repertoire between these two cells. She found an active viral genome expression (both early and late genes) in 3A trophoblastic cells previously cultured with HPV 16,18,11,31. Moreover she found, in different in-vitro studies, that HPV-31 infection and HPV-16 E6 and E7 oncogenes caused both a decrease in 3A trophoblastic cells number and a low trophoblast-endometrial cells adhesion in the first week after the exposure [12, 13]. The evidence that HPV-16 is able to complete its life cycle in trophoblastic cells was previously reported by Liu et al. [21]. These findings provided to expand HPV biology, to support the hypothesis of a possible link between HPV and some spontaneous abortions, and to search a new technology for studying HPV.

These effects were also confirmed by Gomez et al. who found a 3- to 6- fold greater rate of apoptosis in trophoblastic cells transfected with a plasmid containing the entire HPV-16 genome and a progressive decrease of trophoblast invasion ability (25.2-57.6%) from day 3 until day 15 after transfection compared to negative controls [9]. Also Hong et al. showed a similar trend with a reduction both of implantation rate (less 37.2%) and of migratory/invasive activity in embryos exposed to HPV-16 [7].

The reasons which could explain the reduction of invasiveness of trophoblastic cells were suggested by Boulenouar et al. who found a down-regulation of E-cadherin (a fundamental protein for an adequate cell-to-cell adhesion) in trophoblastic cells expressing HPV-16 viral genome [8].

Although all the considered studies have important limitations (which should not be underestimated) linked to the in-vitro artificial and experimental conditions, most of the analyzed data suggested a possible adverse effect of HPV infection in early pregnancy development and maybe in idiopathic couple infertility. The demonstration that also the spermatozoa can act as a vector of HPV viral genome into oocyte [20] force the scientific community to understand what may be the clinical implication of this discovery. In fact, in 2010 Syrjanen reported that peri-conceptual transmission could theoretically occur via infected oocyte or spermatozoa [22]. So, although currently no studies exist on HPV detection in oocytes, theoretically, subsequent virus transmission might originate from the embryos soon after fertilization (such as via spermatozoa carrier) [20, 22].

This fact acquires an even greater importance since the recent estimated prevalence of HPV sperm infection is about 10% (95% CI:7–14%) in general male population and 16% (95% CI:10–23%) in men affected by unexplained infertility [23].

So, focusing the investigations on HPV implications in human reproduction, it is mandatory to shift the older concept of infection with female gender target (i.e. oncologic risk in infected women respect to men) and to start in considering the HPV infection as a couple or, even better, a men problem.

In agreement with this new conception, it is intuitive that all the available in-vivo studies are not useful to completely understand the HPV exact role in human infertility because study methods, patients selection and idea conception seem to be inadequate.

The biggest limitation of the in-vivo studies is due to the inappropriate timing of HPV effects evaluation since evidence about in-vitro studies strongly suggests that a large part of HPV negative effects are carried out during a very early stage of embryo development (within the first two weeks after conception). These effects are very difficult to be demonstrated by clinical studies since it is possible to detect a causal-effects ratio on human reproduction only starting from the third week after conception (five week of amenorrhea). In this way all clinical studies lose a large part of negative effects demonstrated by in-vitro experimental studies.

Anyway clinical evidence can elucidate the consequences of HPV in late embryos development and pregnancy evolution. The detection of HPV in the placental tissue [24] lead to speculate about its possible role in adverse pregnancy outcomes since only few recent studies find an association between viral detection, placental abnormalities and preterm delivery [9, 25, 26]. Despite the increasing evidence of HPV vertical transmission [27, 28], this route is regarded as less clinically important because of the detections of transient HPV-DNA. However, recent studies have provided clear evidence of papillomavirus productive infection in lymphocytes and placenta [29]. Furthermore, a model of papillomavirus latency has been recently proposed that could explain the failure or transience in HPV detection observed in some infected infants. This new evidence of hematogeneous and vertical spread of HPV suggests that these modes of transmission should be investigated in greater detail to obtain a better understanding of the infection and a fuller awareness of the preventive measures that can be taken against HPV-related diseases [30].


In conclusion all the efforts of the scientific community to investigate the real role of HPV in human reproduction disorders cannot underestimate the severe BIAS of previous evidence in postulating new hypothesis and research projects. Even if the choice of more appropriate laboratory techniques (ISH rather than PCR) could partially solve the BIAS linked to potential contamination of specimen, shifting the attention on men and couples rather than only on women represent a first step to solve the dilemma. As suggestion to Clinicians interested in the topic we invite to focus the attention on idiopathic infertile couples undergoing ART cycles, theoretically the most appropriate cohort to plan both in-vitro and in-vivo further studies.

We must definitively understand if the hypothesized adverse effects of HPV in human reproduction is only a supposition derived from a “inconclusive” scientific speculation or if we are faced to a new important discovery which can potentially clarify the exact mechanism of some cases of unexplained couples infertility and of early miscarriages linked to HPV infection.

So If the suspected HPV role in early human reproduction impairment will be confirmed by well conducted further studies, the couple vaccination before attempting both spontaneous and assisted pregnancy could be a reliable and effective tool [31].

The rationale for proposing the use of HPV vaccination (Gardasil® or Cervarix®) in couple attempting ART cycle is based on the evidence that in man the HPV sperm infection seems associated with some spermatic parameters impairment [1] and in women HPV vaccination strength the immunological response to the HPV genotype already detected preventing de novo coinfection and superinfection by a different hr-HPV and lr-HPV genotypes [31]. As theoretical assumption, couple vaccination may potentially reduce some “undetected early miscarriage” actually erroneous considered as ART failure (lack of embryos implantation) increasing the pregnancy rate (first aim of ART procedures).

If in infertile couple the fertility rate will result increased after vaccination, this can be considered an indirect confirmation of our hypothesis and a suggestion to start more appropriate in-vitro and epidemiological studies on this field.

Improvement in the knowledge of HPV-DNA sperm infection mechanisms, timing, and link to fertility impairment may explain some of the actual “idiopathic” male and couple infertility.


  1. Gizzo S, Ferrari B, Noventa M, Ferrari E, Patrelli TS, Gangemi M, Nardelli GB: Male and couple fertility impairment due to HPV-DNA sperm infection: update on molecular mechanism and clinical impact-systematic review. Biomed Res Int. 2014, 2014: 230263-

    PubMed Central  PubMed  Google Scholar 

  2. Hermonat PL, Han L, Wendel PJ, Quirk JG, Stern S, Lowery CL, Rechtin TM: Human papillomavirus is more prevalent in first trimester spontaneously aborted products of conception compared to elective specimens. Virus Genes. 1997, 14: 13-17. 10.1023/A:1007975005433.

    Article  CAS  PubMed  Google Scholar 

  3. Perino A, Giovannelli L, Schillaci R, Ruvolo G, Fiorentino FP, Alimondi P, Cefalù E, Ammatuna P: Human papillomavirus infection in couples undergoing in vitro fertilization procedures: impact on reproductive outcomes. Fertil Steril. 2011, 95: 1845-1848. 10.1016/j.fertnstert.2010.11.047.

    Article  PubMed  Google Scholar 

  4. Skoczyński M, Goździcka-Józefiak A, Kwaśniewska A: Prevalence of human papillomavirus in spontaneously aborted products of conception. Acta Obstet Gynecol Scand. 2011, 90: 1402-1405. 10.1111/j.1600-0412.2011.01189.x.

    Article  PubMed  Google Scholar 

  5. Conde-Ferráez L, Chan May Ade A, Carrillo-Martínez JR, Ayora-Talavera G, González-Losa Mdel R: Human papillomavirus infection and spontaneous abortion: a case–control study performed in Mexico. Eur J Obstet Gynecol Reprod Biol. 2013, 170: 468-473. 10.1016/j.ejogrb.2013.07.002.

    Article  PubMed  Google Scholar 

  6. Ticconi C, Pietropolli A, Fabbri G, Capogna MV, Perno CF: Piccione E. Recurrent miscarriage and cervical human papillomavirus infection. Am J Reprod Immunol. 2013, 70: 343-346.

    CAS  PubMed  Google Scholar 

  7. Hong LJ, Oshiro BT, Chan PJ: HPV-16 exposed mouse embryos: a potential model for pregnancy wastage. Arch Gynecol Obstet. 2013, 287: 1093-1097. 10.1007/s00404-013-2711-5.

    Article  PubMed  Google Scholar 

  8. Boulenouar S, Weyn C, Van Noppen M, Moussa Ali M, Favre M, Delvenne PO, Bex F, Noël A, Englert Y, Fontaine V: Effects of HPV-16 E5, E6 and E7 proteins on survival, adhesion, migration and invasion of trophoblastic cells. Carcinogenesis. 2010, 31: 473-480. 10.1093/carcin/bgp281.

    Article  CAS  PubMed  Google Scholar 

  9. Gomez LM, Ma Y, Ho C, McGrath CM, Nelson DB, Parry S: Placental infection with human papillomavirus is associated with spontaneous preterm delivery. Hum Reprod. 2008, 23: 709-715. 10.1093/humrep/dem404.

    Article  CAS  PubMed  Google Scholar 

  10. Henneberg AA, Patton WC, Jacobson JD, Chan PJ: Human papilloma virus DNA exposure and embryo survival is stage-specific. J Assist Reprod Genet. 2006, 23: 255-259. 10.1007/s10815-006-9030-8.

    Article  PubMed Central  PubMed  Google Scholar 

  11. Weyn C, Vanderwinden JM, Rasschaert J, Englert Y, Fontaine V: Regulation of human papillomavirus type 16 early gene expression in trophoblastic and cervical cells. Virology. 2011, 412: 146-155. 10.1016/j.virol.2010.12.056.

    Article  CAS  PubMed  Google Scholar 

  12. You H, Liu Y, Agrawal N, Prasad CK, Chiriva-Internati M, Lowery CL, Kay HH, Hermonat PL: Infection, replication, and cytopathology of human papillomavirus type 31 in trophoblasts. Virology. 2003, 316: 281-289. 10.1016/j.virol.2003.08.020.

    Article  CAS  PubMed  Google Scholar 

  13. You H, Liu Y, Agrawal N, Prasad CK, Edwards JL, Osborne AF, Korourian S, Lowery CL, Hermonat PL: Multiple human papillomavirus types replicate in 3A trophoblasts. Placenta. 2008, 29: 30-38. 10.1016/j.placenta.2007.08.005.

    Article  CAS  PubMed  Google Scholar 

  14. Cabrera M, Chan PJ, Kalugdan TH, King A: Transfection of the inner cell mass and lack of a unique DNA sequence affecting the uptake of exogenous DNA by sperm as shown by dideoxy sequencing analogues. J Assist Reprod Genet. 1997, 14: 120-124. 10.1007/BF02765781.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  15. Calinisan JH, Chan SR, King A, Chan PJ: Human papillomavirus and blastocyst apoptosis. J Assist Reprod Genet. 2002, 19: 132-136. 10.1023/A:1014736805127.

    Article  PubMed Central  PubMed  Google Scholar 

  16. Matovina M, Husnjak K, Milutin N, Ciglar S, Grce M: Possible role of bacterial and viral infections in miscarriages. Fertil Steril. 2004, 81: 662-669. 10.1016/j.fertnstert.2003.08.020.

    Article  CAS  PubMed  Google Scholar 

  17. Eppel W, Worda C, Frigo P, Ulm M, Kucera E, Czerwenka K: Human papillomavirus in the cervix and placenta. Obstet Gynecol. 2000, 96: 337-341. 10.1016/S0029-7844(00)00953-4.

    Article  CAS  PubMed  Google Scholar 

  18. Rombaldi RL, Serafini EP, Mandelli J, Zimmermann E, Losquiavo KP: Transplacental transmission of Human Papillomavirus. Virol J. 2008, 5: 106-10.1186/1743-422X-5-106.

    Article  PubMed Central  PubMed  Google Scholar 

  19. Saccardi C, Gizzo S, Noventa M, Anis O, Di Gangi S, Patrelli TS, D’Antona D, Nardelli GB: High-risk human papillomavirus DNA test: could it be useful in low-grade cervical lesion triage? Five-year follow-up. Reprod Sci. 2014, 21: 198-203. 10.1177/1933719113492214.

    Article  PubMed  Google Scholar 

  20. Foresta C, Patassini C, Bertoldo A, Menegazzo M, Francavilla F, Barzon L, Ferlin A: Mechanism of human papillomavirus binding to human spermatozoa and fertilizing ability of infected spermatozoa. PLoS One. 2011, 6: e15036-10.1371/journal.pone.0015036.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  21. Liu Y, You H, Chiriva-Internati M, Korourian S, Lowery CL, Carey MJ, Smith CV, Hermonat PL: Display of complete life cycle of human papillomavirus type 16 in cultured placental trophoblasts. Virology. 2001, 290: 99-105. 10.1006/viro.2001.1135.

    Article  CAS  PubMed  Google Scholar 

  22. Syrjänen S: Current concepts on human papillomavirus infections in children. APMIS. 2010, 118: 494-509. 10.1111/j.1600-0463.2010.02620.x.

    Article  PubMed  Google Scholar 

  23. Laprise C, Trottier H, Monnier P, Coutlée F, Mayrand MH: Prevalence of human papillomaviruses in semen: a systematic review and meta-analysis. Hum Reprod. 2014, 29: 640-651. 10.1093/humrep/det453.

    Article  PubMed  Google Scholar 

  24. Weyn C, Thomas D, Jani J, Guizani M, Donner C, Van Rysselberge M, Hans C, Bossens M, Englert Y, Fontaine V: Evidence of human papillomavirus in the placenta. J Infect Dis. 2011, 203: 341-343. 10.1093/infdis/jiq056.

    Article  PubMed Central  PubMed  Google Scholar 

  25. Zuo Z, Goel S, Carter JE: Association of cervical cytology and HPV DNA status during pregnancy with placental abnormalities and preterm birth. Am J Clin Pathol. 2011, 136: 260-265. 10.1309/AJCP93JMIUEKRPIW.

    Article  PubMed  Google Scholar 

  26. Kim YM, Chaiworapongsa T, Gomez R, Bujold E, Yoon BH, Rotmensch S, Thaler HT, Romero R: Failure of physiologic transformation of the spiral arteries in the placental bed in preterm premature rupture of membranes. Am J Obstet Gynecol. 2002, 187: 1137-1142.

    Article  PubMed  Google Scholar 

  27. Hahn HS, Kee MK, Kim HJ, Kim MY, Kang YS, Park JS, Kim TJ: Distribution of maternal and infant human papillomavirus: risk factors associated with vertical transmission. Eur J Obstet Gynecol Reprod Biol. 2013, 169: 202-206. 10.1016/j.ejogrb.2013.02.024.

    Article  CAS  PubMed  Google Scholar 

  28. Lee SM, Park JS, Norwitz ER, Koo JN, Oh IH, Park JW, Kim SM, Kim YH, Park CW, Song YS: Risk of vertical transmission of human papillomavirus throughout pregnancy: a prospective study. PLoS One. 2013, 8: e66368-10.1371/journal.pone.0066368.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  29. Foresta C, Bertoldo A, Garolla A, Pizzol D, Mason S, Lenzi A, De Toni L: Human papillomavirus proteins are found in peripheral blood and semen Cd20+ and Cd56 + cells during Hpv-16 semen infection. BMC Infect Dis. 2013, 13: 593-10.1186/1471-2334-13-593.

    Article  PubMed Central  PubMed  Google Scholar 

  30. Freitas AC, Mariz FC, Silva MA, Jesus AL: Human papillomavirus vertical transmission: review of current data. Clin Infect Dis. 2013, 56: 1451-1456. 10.1093/cid/cit066.

    Article  CAS  PubMed  Google Scholar 

  31. Gizzo S, Noventa M, Nardelli GB: Gardasil administration to hr-HPV-positive women and their partners. Trends Pharmacol Sci. 2013, 34: 479-480. 10.1016/

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations


Corresponding author

Correspondence to Salvatore Gizzo.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

MN & SG carried out literature search, critical analysis of data and written the manuscript. AA carried out language revision and critical comment. GBN and GA participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.

Rights and permissions

Open Access  This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made.

The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.

To view a copy of this licence, visit

The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Noventa, M., Andrisani, A., Gizzo, S. et al. Is it time to shift the attention on early stages embryo development to avoid inconclusive evidence on HPV-related infertility: debate and proposal. Reprod Biol Endocrinol 12, 48 (2014).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: