Impact of Cryopreservation Methods on Post-Thaw SARS-CoV-2 in Semen Samples

The pandemic caused by SARS-CoV-2 ranks among the most devastating events in recent history. Limited knowledge exists regarding the characteristics and behavior of this beta coronavirus, particularly its potential impact on reproductive medicine. Questions remain about the presence of the virus in seminal fluid and whether male semen could serve as a transmission route. Additionally, concerns exist about the virus impairing male reproductive potential through fever or the "cytokine storm" triggered by the immune response.

No current evidence confirms whether SARS-CoV-2 can survive semen cryopreservation, though other viruses, such as influenza, have demonstrated survival in liquid nitrogen freezing. Semen cryopreservation is a critical fertility preservation strategy for conditions like cancers, autoimmune diseases, or cryptorchidism. The contamination of cryopreserved semen by SARS-CoV-2 could turn such samples into hazardous viral reservoirs.

The study aims to investigate the presence of the virus in semen, identify cells expressing viral receptors ACE2 and TMPRSS2, and evaluate the virus's direct and indirect effects on male reproductive capacity. Objectives include determining if SARS-CoV-2 survives cryopreservation procedures and identifying optimal methods to ensure virus-free cryopreserved semen while separating infected material from male gametes.

The study will recruit 20 men exposed to SARS-CoV-2 and 20 control subjects, all treated at the Humanitas Fertility Center, Department of Gynecology, at the Humanitas Research Hospital. Each participant will provide a semen sample for evaluation. This observational study will not involve clinical interventions or alter regular diagnostic procedures.

Participants undergoing routine tests for medically assisted reproduction and deemed eligible after completing an anamnesis questionnaire will be included. Samples will be processed in the Mucosal Immunology and Microbiota Unit at the Humanitas Clinical Institute.

Using cell biology, molecular biology, and flow cytometry techniques, the study will assess viral contamination, receptor expression in spermatozoa, and inflammatory cytokine levels in seminal fluid after two cryopreservation methods: slow two-step freezing and vitrification. Analyses will cover unprocessed semen and samples exposed in vitro to SARS-CoV-2 under BSL3 conditions.

Additionally, the cellular fraction of semen, including granulocytes, lymphocytes, round cells, and spermatozoa, will undergo phenotype and activation state characterization. The study will evaluate viral contamination in cryopreserved semen and assess the effectiveness of protocols designed to separate infected material from male gametes.

Inclusion criteria

Patient population inclusion criteria:

• • Male subjects, aged 18-50 requiring a semen fluid evaluation.

• Positive IgG serological test result performed not more than 3 months before recruitment
• Signed informed consent
• Anamnestic test compilation

Control subject inclusion criteria:

• Male subjects, aged 18-50 requiring a semen fluid evaluation.
• Negative IgG serological test result performed within the last month
• Signed informed consent
• Anamnestic test compilation

Exclusion criteria

• Patient population exclusion criteria:

• Severe male Factor (azoospermia and <200,00 sperm per ejaculate)
• Fever (>38.5 C) in the 60 days before enrollment
• Treated with antibiotic at the time of enrolment or two months before enrolment
• Treated with cortisone at the time of enrolment or two months before enrolment

Control subject population exclusion criteria:

• Severe male Factor (azoospermia and <200,00 sperm per ejaculate)
• Fever (>38.5 C) in the 60 days before enrolment
• Known history of SARS-CoV-2 infection
• Treated with antibiotic at the time of enrolment or two months before enrolment
• Treated with cortisone at the time of enrolment or two months before enrolment