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Rago, V.; Perri, A. SARS-CoV-2 Infection and the Testis. Encyclopedia. Available online: https://encyclopedia.pub/entry/41969 (accessed on 01 July 2024).
Rago V, Perri A. SARS-CoV-2 Infection and the Testis. Encyclopedia. Available at: https://encyclopedia.pub/entry/41969. Accessed July 01, 2024.
Rago, Vittoria, Anna Perri. "SARS-CoV-2 Infection and the Testis" Encyclopedia, https://encyclopedia.pub/entry/41969 (accessed July 01, 2024).
Rago, V., & Perri, A. (2023, March 08). SARS-CoV-2 Infection and the Testis. In Encyclopedia. https://encyclopedia.pub/entry/41969
Rago, Vittoria and Anna Perri. "SARS-CoV-2 Infection and the Testis." Encyclopedia. Web. 08 March, 2023.
SARS-CoV-2 Infection and the Testis
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This entry is adapted from the peer-reviewed paper 10.3390/life13020586

Many studies have suggested that SARS-CoV-2, directly or indirectly, can affect the male reproductive system, although the underlined mechanisms have not been completely elucidated yet. The main data regarding the morphological alterations in the testes emerged from autoptic studies that revealed interstitial congestion, micro thrombosis, reduction of Sertoli, Leydig, and germinal cells, infiltrated immune cells, and atrophic seminiferous tubules consistent with orchitis. Furthermore, men with severe infection exhibit sperm parameter alterations, together with abnormalities of the hypothalamic–pituitary–testis axis, strongly suggesting that SARS-CoV-2 could increase the risk of male infertility.

SARS-CoV-2 COVID-19 fertility

1. Introduction

The interest of the researchers toward the possible influences of COVID-19 on male fertility arises from the evidence that testis express ACE2 and TMPRSS2, including spermatogonia, peritubular myoid cells, testis somatic cells, and spermatogonial stem cells [1]. However, studies based on single-cell RNA sequencing did not find ACE2/TMPRSS2 co-expression in any type of testicular tissue [2], hence, the direct capacity of SARS-CoV-2 to promote direct testicular damage is a still debated issue. Notably, a recent study reported that when TMPRSS2 is not expressed or has low expression, SARS-CoV-2 enters the host cells through the endosomal pathway, using ACE2 and cathepsins [3]. In addition, inflammatory cytokines and oxidative stress SARS-CoV-2-induced can affect Leydig cells, disrupting their capacity to produce testosterone, and germinal cells, hindering spermatogenesis [4]. Finally, Geslot, A et al. described a hypothalamic pathology resulting from SARS-CoV-2-related neuroinflammation, which can alter testicular function, affecting gonadotropins secretion [5].
The data regarding the impact of SARS-CoV-2 infection on testicular function mainly arises from a few autoptic studies performed on testis and epididymis specimens of dead patients with COVID-19. Although the evidence regarding the presence of the virus in the testes is remarkably discordant, unanimous information is available on the macro and microscopic damage to the testes. The study of Ma et al. evaluated the detrimental effects of SARS-CoV-2 infection by examining the molecular features of testes obtained from COVID-19 patients [6]. The authors found numerous apoptotic germ cells concomitant with a significant number of infiltrated immune cells in the interstitial compartments, and they also observed plasma cells and activated B cells, suggesting that SARS-CoV-2 might trigger a secondary autoimmune response, in addition to the primary pathogenesis of viral orchitis [6]. Furthermore, the authors found an elevated expression of ACE2 and TMPRSS2 in the seminiferous tubules of all patients, supporting the hypothesis that SARS-CoV-2 could directly attack testicular cells. Finally, they evaluated the transcriptome changes in all patients’ testes, establishing, by Gene Ontology analysis, the activation of some inflammation-related processes and the downregulation of genes implicated in spermatogenesis [6]. The hypothesis that the elevated testicular immune response could cause impaired sperm parameters and testicular damage, has been further supported by the study of Li et al., who reported edema, interstitial congestion, and red blood cells at the autopsy of testicular and epididymal samples from patients who died from COVID-19 [7]. Moreover, the authors found elevated seminal levels of IL-6 and TNF-α, suggesting an autoimmune origin of orchitis [7]. Extensive germ cell damage has been also described by Yang et al., who concomitantly observed detachment of Sertoli cells from the tubular basement membrane, leukocyte infiltration, and a reduced number of Leydig cells [8]. Similar results have been reported by other autoptic studies showing signs of acute damage, including sloughing of spermatocytes, swelling of Sertoli cells, microthrombosis in the testicular vasculature, increase in apoptotic cells within seminiferous tubules, and increased infiltration of CD3+ T lymphocytes and CD68+ macrophages in testicular interstitium [7][8][9]. Interestingly, the retrospective study of Chen et al., including 142 patients positive for COVID-19 who underwent scrotal ultrasound at diagnosis, revealed that about 22% were found to have increased tunica thickness and increased vascular flow consistent with orchitis, epididymitis, or epididymo-orchitis [10].

2. SARS-CoV-2 in the Semen and Sperm Parameters in COVID-19 Patients

The presence of SARS-CoV-2 in the semen represents a noteworthy, debated topic in the literature. Two recent systematic reviews and meta-analyses reported that SARS-CoV-2 viral RNA is undetectable in the semen samples of COVID-19 patients with active infections or in those who have recovered; conversely, only two studies documented semen viral mRNA detection in a relevant number of patients [11][12]. With respect to this topic, Corona G et al. speculated that the seminal identification of the virus in the early phase of the infection can be the consequence of the alteration of the blood–testicular barrier, or its excretion in the seminal fluid. In addition, the authors highlighted that the majority of available studies provided limited information regarding the method of semen collection and preparation. It is well known that a correct semen sampling method is crucial, as the detection of virus in the semen could reflect contamination from feces, urine, hands, or respiratory droplets [13]. The sensitivity and specificity of the RT-PCR methods used to detect SARS-CoV-2 in seminal fluid is a very important issue [14]. Paoli D et al. performed a new qualitative determination of the RT-PCR assays in different fractions of seminal fluid from patients with COVID-19, confirming the feasibility of this test for the molecular diagnosis of SARS-CoV-2 in seminal fluid [15]. The potential risk of sexual transmission and semen contamination of SARS-CoV-2 remains an open question, being particularly relevant for the cryopreservation and use of male gametes in Assisted Reproduction Technology (ART) procedures. Currently, although no global guidelines are provided, as well as data on the minimum required interval between COVID-19 recovery and ART, many scientific societies affirmed the importance of continued reproductive care during the COVID-19 pandemic, concomitantly recommending caution to couples planning natural pregnancy or ART [16].
The studies evaluating the effects of COVID-19 on semen parameters compared to healthy controls demonstrated that COVID-19 was associated with a significant reduction of total sperm count, sperm concentration, and total motility, together with a lower seminal volume, whereas no difference in sperm morphology or progressive motility was observed [11]. Conversely, the results of Pazir’s study conducted among 24 subjects before and after SARS-CoV-2 infection demonstrated a significant decrease in total motility and total motile sperm count [17].
Interestingly, Hajizadeh Maleki et al. found higher levels of seminal ACE2 enzymatic activity, oxidative stress, and pro-and anti-inflammatory cytokines. In addition, the authors observed considerable cytopathological alterations, DNA damage, and apoptosis in the sperm cells, amounting to a transient state of male subfertility such as that with oligoasthenoteratozoospermia. Similarly, the study of Li et al., which has been conducted among 23 hospitalized COVID-19 patients, demonstrated that more than one-third have sperm density reduction concomitant with increased levels of leukocytes and inflammatory factors compared to controls [7]. Furthermore, the disruption of the blood–testis barrier involving Sertoli cells caused by the cytokine storm could promote the production of anti-sperm antibodies, whose presence is known to be associated with lower sperm concentration and motility [18]. The recent meta-analysis conducted by Yudhistira Pradnyan Kloping et al. compared the results between patients with different degrees of severity, showing that the patients with more severe infections had worse sperm analysis results, both in concentration between mild and moderate, mild and severe, as well as moderate and severe infections, and mean semen volume between moderate and severe infections [12]. The reasons behind these findings may depend on different and concomitant factors, including the direct local damage caused by the virus and the systemic effect. In particular, the elevated body temperature observed in severe cases, as well as the cytokine storm, promote deleterious effects on sperm count and motility [19][20][21][22]. The study conducted by Donders et al. reported that sperm parameters were mostly severely damaged when assessed during the first month after COVID-19 infection and were less pronounced and almost normal in men tested after more than 1 and 2 months, respectively, suggesting a tendency of COVID-19-related sperm impairment towards reversibility [23]. In this regard, Paoli D et al. performed a seminological evaluation three months after COVID-19 recovery, demonstrating that semen parameters and sperm DNA fragmentation presented no significant long-term impairment, and no sperm autoimmune response was detected. The authors stress the concept that SARS-CoV-2 can temporarily affect spermatogenesis and that when sperm analysis is conducted after a complete spermatogenetic cycle, during approximately 78 days, alterations in seminal parameters are no longer noticeable. Against this background, the authors suggested that it is possible to counsel infertile couples to postpone ART procedures for around three months after recovery from the infection [24].
One limitation of the studies exploring the changes in semen quality in the above-reported patients with COVID-19 is the lack of pre-infection data since the referent point is the comparisons with uninfected controls. Furthermore, an important topic is how long after infection the seminal changes persist. A new scenario seems to be opened by recent studies demonstrating recovery at three months after infection. Therefore, similar further multicentric studies in that regard should be performed in order to confirm that the seminological changes are transient, as well as the general damage of the testes.
In addition, these studies should be designed to better establish whether and to what extent the changes correlate with the severity degree, strengthening the relevance of SARS-CoV-2-related systemic inflammation in the development of the testicular dysfunction.

3. COVID-19 Vaccination and Semen Parameters

Recently, the possible impact of COVID-19 vaccination on semen parameters in healthy men appears to be a remarkable concern. Gonzalez et al. reported that mRNA vaccines (BNT162b2/Pfizer-BioNTech and mRNA-1273/Moderna) did not promote statistically significant changes in any sperm parameters after vaccination [25]. The recent longitudinal study of Gat et al. aimed to investigate the effect of the COVID-19 BNT162b2 (Pfizer) vaccine on semen parameters among semen donors. The authors demonstrated a selective temporary decline in sperm concentration and total motile count three months post-vaccination, followed by recovery, strengthening the need for further studies on different vaccines and populations, particularly in sub-fertile patients [26]. Finally, the recent narrative review of Pourmasumi et al. reported that no impairment of reproductive function caused by vaccines has been demonstrated [27]. Therefore, starting from the evidence emerging from the available clinical trials, the medical community should reassure the public about the safety of vaccination to prevent the negative effects of COVID-19 also on male fertility.

4. Hypothalamic–Pituitary–Testes in COVID-19 Patients

A further aspect that should be considered is that SARS-CoV-2 has been shown to cross the blood–brain barrier, and when infecting ACE2-expressing cells, it promotes neuroinflammation in brain regions, including the hypothalamus, leading to the disruption of its physiological functions of temperature regulation and hormone balance [28][29]. Therefore, the increased risk of male infertility observed in patients with COVID-19 could also be addressed by the dysfunction of the hypothalamic–pituitary–testes axis, which causes the abnormal secretion of GnRH, LH, and FSH, affecting testosterone production and spermatogenesis. However, although hypogonadism resulting from inflammation in the testes is increasingly evident [30][31], to date, few studies have investigated the contribution of hypothalamic dysfunction. Some studies report increased circulating levels of gonadotropins in men with COVID-19, mainly in those with more severe disease, speculating that these findings could be the consequence of the transient activation of the gonadotropin-secreting cells due to early inflammatory responses [32][33]. In addition, it should be considered that damaged Leydig cells after SARS-CoV-2 infection can reduce testosterone secretion, which may eventually lead to an increase in gonadotropin levels through pituitary feedback. Researchers have evaluated the androgen circulating levels in COVID-19 patients, sometimes showing different results. In contrast to the analysis proposed by Ma et al., in which no statistical difference in testosterone levels in COVID-19 men compared to non-infected control men have been observed, Rastrelli et al. observed that men with severe COVID-19 infection or dead patients have lower serum testosterone levels than men who have recovered clinically [34]. Similar findings emerge from the retrospective study of Schroeder et al., showing that severe COVID-19 in men is associated with reduced androgen levels [35]. Analogously, Kadihasanoglu et al. discovered that serum LH levels are higher in COVID-19 patients than in controls, while testosterone levels are lower and were negatively correlated with hospitalization time [36]. In agreement with the aforementioned studies, the recent prospective offered by Ertas et al. demonstrates that serum testosterone levels are lower and serum LH levels higher in COVID-19 patients when compared to the control group [37]. Finally, the recent systematic review and meta-analysis of Corona G et al., highlights that low testosterone levels observed in the acute phase of the COVID-19 was associated with an increased risk of being admitted to the intensive care unit or death [11].

References

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  2. Stanley, K.E.; Thomas, E.; Leaver, M.; Wells, D. Coronavirus Disease-19 and Fertility: Viral Host Entry Protein Expression in Male and Female Reproductive Tissues. Fertil. Steril. 2020, 114, 33–43.
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