SARS-CoV-2 infection is detrimental to pregnancy outcomes after embryo transfer in IVF/ICSI: a prospective cohort study

SARS-CoV-2 infection affects not only the health of people all over the world but also the reproductive health of women. The viral spike (S) protein of SARS-CoV-2 plays a crucial role in virus infection. The described mechanism involves viral spike (S) protein-mediated recognition and binding to the angiotensin 1-converting enzyme 2 (ACE2) receptor on the host cell, after which the protease transmembrane serine protease 2 (TMPRSS2) cleaves the S protein to facilitate cell entry [1, 2]. An alternative ACE2-independent mechanism exists, with basigin (BSG or CD147) acting as the cellular receptor and cysteine protease cathepsin L (CTSL) as the protease, potentially mediating SARS-CoV-2 cell entry [1, 2]. Tissues and cells that express these receptors and proteases, particularly those with high co-expression of ACE2 and TMPRSS2, are likely to be more vulnerable to SARS-CoV-2 infection. Previous studies detected low percentages of SARS-CoV-2 virus in female vaginal secretions (5.7–12.5%) and cervical secretions (10.53%) [3‐5]. Due to the limitation of virus detection technology, the current clinical practice often indirectly infers the impact of SARS-CoV-2 infection on different organs by detecting SARS-CoV-2 receptors in different tissues [6]. Previous literature has confirmed that SARS-CoV-2 receptors (classical/nonclassical) are expressed in the female reproductive system (endometrium, ovaries) [1, 7, 8], meaning there is a theoretical possibility that the female reproductive system may be affected by viral infections.

Previous research has established that SARS-CoV-2 infection during controlled ovarian stimulation (COS) may influence embryo development [9, 10]. Some studies have also confirmed that SARS-CoV-2 infection in pregnancy is associated with increases in severe maternal morbidity, mortality, and neonatal complications [11, 12]. It remains controversial whether SARS-CoV-2 infection has adverse effects on early pregnancy outcomes [13, 14]. Previously published articles have shown that the recovery from SARS-CoV-2 infection does not affect pregnancy outcomes in fresh cycles with embryo transfer [15]. Additionally, SARS-CoV-2 vaccination has been found to not negatively affect ovarian function during assisted reproductive technology (ART) outcomes [16, 17]. Despite the available literature, there is a lack of research on whether SARS-CoV-2 infection affects early pregnancy outcomes shortly after an embryo transfer in in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI). Therefore, the main purpose of this study is to explore whether SARS-CoV-2 infection in the short term after embryo transfer is detrimental to pregnancy outcomes.

A total of 1393 patients underwent embryo transfer between December 1 and December 31, 2022. Out of these, 63 patients had a history of SARS-CoV-2 infection before embryo transfer (time interval 1–109 days) and were excluded from the analysis. The final dataset included 1330 patients, divided into the following three groups: 51.6% (n = 687) were in the SARS-CoV-2 diagnosed group, 16.4% (n = 219) in the SARS-CoV-2 suspected infection group, and 32% (n = 424) in the uninfected group. The basic characteristics of the patients in the three groups, including age and the presence of special diseases such as polycystic ovary syndrome (PCOS), endometriosis, adenomyosis, intrauterine adhesions, obesity, and diabetes, as well as the rate of top-quality embryo transfer, were not significantly different. The clinical pregnancy rate was 68% in the SARS-CoV-2 diagnosed group, 63% in the uninfected group, and 51% in the suspected infection group (P < 0.001) (Table 1). The ongoing pregnancy rate was 58% in the SARS-CoV-2 diagnosed group, 53% in the uninfected group, and 45% in the suspected infection group (P < 0.001) (Table 1). There was no significant difference in biochemical pregnancy rate, early miscarriage rate, or ectopic pregnancy rate (Table 1).

Analysis of vaccination and SARS-CoV-2 infection information showed that the SARS-CoV-2 diagnosed group and suspected infection group had a comparable vaccination rate (83% vs 84%). The proportion of patients with a shorter time interval (14–21 days) between embryo transfer and SARS-CoV-2 infection was higher in the SARS-CoV-2 suspected infection group (38% vs 25%, P < 0.001) than in the diagnosed group (Table 2). There were higher proportions of symptoms with fever (60% vs 68%, P = 0.032), dizziness/headache (34% vs 43%, P = 0.022), or loss of appetite (19% vs 28%, P = 0.007) in the suspected infection group compared to the diagnosed group (Table 2). Although not statistically significant, the incidence of cough (76% vs 74%), sore throat (39% vs 34%), and muscle soreness (45% vs 47%) in the SARS-CoV-2 suspected infection group was higher than in the diagnosed group (Additional file 1: Table S1).

Logistic regression analysis was performed to explore the factors affecting clinical pregnancy. There were no statistically significant differences in the basic characteristics between the clinical pregnancy group and the non-pregnancy group (Additional file 2: Table S2). However, vaccination (OR 1.513, 95% CI 1.134–2.019, P = 0.005), especially three doses of the vaccine (OR 1.804, 95% 1.332–2.444, P < 0.001), can help improve the clinical pregnancy rate compared to unvaccinated individuals (Table 3). Suspected infection status decreased the clinical pregnancy rate by 38.2% (OR 0.618, 95% CI 0.444–0.862, P = 0.005) compared to the uninfected group. A longer time interval between embryo transfer and SARS-CoV-2 infection was associated with a higher clinical pregnancy rate (OR 1.022, 95% CI 1.001–1.043, P = 0.042) (Table 3). Receiver operating characteristic (ROC) analysis identified the cutoff value of 22 days as a predictor for the interval time between embryo transfer and SARS-CoV-2 infection (OR 3.76 95% CI 1.92–8.24, P < 0.001) (Additional file 3: Fig. S1, Additional file 4: Table S3). Although there was no statistical difference in the overall symptoms of SARS-CoV-2 infection, the overall incidence of SARS-CoV-2 symptoms in the pregnancy group was lower (Additional file 5: Table S4). However, SARS-CoV-2 symptoms with the occurrence of fever and dizziness/headache decreased the clinical pregnancy rate by 28.5% (OR 0.715, 95% CI 0.526–0.972, P = 0.032) (Table 3).

This is the first large sample prospective cohort study to explore the impact of SARS-CoV-2 infection in the short term after embryo transfer on pregnancy outcomes. The findings suggest that symptomatic SARS-CoV-2 infection shortly after embryo transfer is not conducive to clinical pregnancy.

Existing published articles have primarily focused on whether SARS-CoV-2 infection during pregnancy affects obstetric outcomes or early miscarriage rate [11‐14, 20]. Currently, the adverse effects of obstetric outcomes are relatively clear, with women diagnosed with COVID-19 being at an increased risk of a composite maternal morbidity and mortality index [11, 12]. However, there is ongoing controversy regarding the early miscarriage rate [13, 14, 20]. Moreover, in the prospective cohort, 18 (1.8%) women had SARS-CoV-2 antibodies in the serum from the double test, which is suggestive of SARS-CoV-2 infection, in early pregnancy [13]. This retrospective case–control study suggested that the early miscarriage rate was nearly 50%, although the population selection may have affected the results [20]. The majority of these studies have focused on non-assisted reproductive technology (non-ART) pregnancies, making it challenging to accurately determine the interval time between SARS-CoV-2 infection and embryo implantation or to determine the impact on women receiving ART [14].

The mechanism of adverse effects of SARS-CoV-2 infection on pregnancy outcomes in the short term after embryo transfer is not fully understood. However, previously published articles suggest that two aspects may be considered. The first mechanism is that SARS-CoV-2 directly infects the embryo, affecting embryonic development. Studies analyzing RNA sequencing data of donated zygotes and blastocysts show that early embryos and late blastocysts express ACE2, while TMPRSS2 is expressed only in late blastocysts, indicating the co-expressed two types of receptors in late blastocysts [21]. Another study utilizing donated human gametes evaluated the expression of SARS-CoV-2 receptor protein on embryos and found that the 5th- and 7th-day blastocysts showed the expression of ACE2 and BSG on the trophoblast and inner cell mass cell membrane, suggesting that SARS-CoV-2 could potentially infect embryos [22]. When human blastocysts are exposed to SARS-CoV-2, both trophoblast cells and inner cell mass cells are infected, displaying signs of cellular degeneration, indicating the pathogenic effect of infection [23]. The zonal pellucida seems to have a protective effect against SARS-CoV-2 infection [23]. During embryo implantation, as the blastocyst hatches and the protective effect of the zona pellucida is removed, the embryo implantation process may be affected by the pathogenic effect of the SARS-CoV-2 virus. The second mechanism involves the potential impact of SARS-CoV-2 infection on maternal immune status. Previous literature suggests that immune cells in the peripheral blood after SARS-CoV-2 infection undergo two-way changes: activation of NK cells and excessive depletion of NK and T cells [24]. The immune status experiences the process of innate immunity, adaptive immunity, and immune tolerance after SARS-CoV-2 infection [24‐27]. Previous studies have found that SARS-CoV-2 infection leads to severe peripheral lymphocyte reduction with decreased numbers of CD4 + T cells, CD8 + T cells, NK cells, and B cells [28]. A study on patients with long COVID found altered T cells, including depleted T cells and reduced CD4 + and CD8 + effector memory cells persisting for 13 months [29]. A comprehensive study comparing patients with long COVID to uninfected individuals and infected individuals without long COVID found increased numbers of non-classical monocytes, activated B cells, and IL-4- and IL-6-secreting CD4 + T cells, as well as exhausted T cells in individuals with long COVID at a median of 14 months after infection [29, 30]. Therefore, SARS-CoV-2 infection may affect clinical pregnancy outcomes by interfering with maternal immune balance.

Our research results suggest that the SARS-CoV-2 diagnosed group does not affect clinical pregnancy significantly, while the suspected infection group was not conducive to pregnancy outcomes. The main difference between these two groups was the presence of symptoms. Analysis of the SARS-CoV-2 diagnosis group found that 95% of the patients had SARS-CoV-2 symptoms, making it impossible to further analyze SARS-CoV-2 infection based on asymptomatic cases. While only fever and dizziness/headache symptoms were found to be not conducive to clinical pregnancy, the overall incidence of symptoms in the non-pregnant group was still significantly higher than that in the pregnant group (Table 3). Based on these observations, we speculated that the symptoms of SARS-CoV-2 infection may indicate the maternal immune response to SARS-CoV-2 infection. Meanwhile, implantation failure is often accompanied by a shift in the phenotypes of immune cells, with a bias toward effector T cells, overactivated or under-activated uNK cells, M1 (pro-inflammatory) macrophages, or immunogenic dendritic cells [31]. Previous literature suggests that severe SARS-CoV-2 infection is accompanied by a T cell response with a delayed cytotoxic reaction [27]. Therefore, we speculated that SARS-CoV-2 infection may lead to changes in immune status at the early stage of embryo implantation, leading to unfavorable conditions for successful embryo implantation. Thus, the possible mechanism of SARS-CoV-2 infection in the short term (≤ 22 days) after embryo transfer is more concerned with changes in the immune state. Moreover, the vaccination for two to three times improves clinical pregnancy, which further supports the above supposition.

The main advantage of this study is the relatively large sample prospective cohort study. In addition, this research explores the real data of the first round of the SARS-CoV-2 infection outbreak in China. It is helpful to understand the influence of SARS-CoV-2 infection on pregnancy outcomes after embryo transfer, and our data suggest that there is no difference in baseline characteristics related to pregnancy outcomes, which makes the conclusion more reliable.

This study explores the impact of SARS-CoV-2 infection symptoms on pregnancy outcomes, which is another advantage as it is a more comprehensive evaluation of the possible impact of SARS-CoV-2 infection on women of childbearing age. Yet, it is also a limitation because all SARS-CoV-2 symptoms are recalled based on oral descriptions provided by patients during consultations. Not all SARS-CoV-2 infection symptoms can be accurately defined through medical testing indicators such as the specific degree of dizziness/headache, which makes exploring the value of SARS-CoV-2 infection symptoms on pregnancy outcomes difficult.

This study confirms that symptomatic SARS-CoV-2 infection shortly after embryo transfer is not conducive to clinical pregnancy. Given this, reproductive physicians should give infertile women appropriate medical advice by recommending them to avoid SARS-CoV-2 infection as much as possible after embryo transfer and that two to three or more doses of SARS-CoV-2 vaccine before pregnancy may help reduce the impact of SARS-CoV-2 infection.