State Key Laboratory of Emerging Infectious Diseases, Carol Yu Centre for Infection, Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Centre for Virology, Vaccinology and Therapeutics, Hong Kong Science and Technology Park, Hong Kong Special Administrative Region, China.
Clin Infect Dis. 2022 Aug 24;75(1):e974-e990. doi: 10.1093/cid/ciac142.
The role of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the pathogenesis of testicular damage is uncertain.
We investigated the virological, pathological, and immunological changes in testes of hamsters challenged by wild-type SARS-CoV-2 and its variants with intranasal or direct testicular inoculation using influenza virus A(H1N1)pdm09 as control.
Besides self-limiting respiratory tract infection, intranasal SARS-CoV-2 challenge caused acute decrease in sperm count, serum testosterone and inhibin B at 4-7 days after infection; and chronic reduction in testicular size and weight, and serum sex hormone at 42-120 days after infection. Acute histopathological damage with worsening degree of testicular inflammation, hemorrhage, necrosis, degeneration of seminiferous tubules, and disruption of orderly spermatogenesis were seen with increasing virus inoculum. Degeneration and death of Sertoli and Leydig cells were found. Although viral loads and SARS-CoV-2 nucleocapsid protein expression were markedly lower in testicular than in lung tissues, direct intratesticular injection of SARS-CoV-2 demonstrated nucleocapsid expressing interstitial cells and epididymal epithelial cells, While intranasal or intratesticular challenge by A(H1N1)pdm09 control showed no testicular infection or damage. From 7 to 120 days after infection, degeneration and apoptosis of seminiferous tubules, immune complex deposition, and depletion of spermatogenic cell and spermatozoa persisted. Intranasal challenge with Omicron and Delta variants could also induce similar testicular changes. This testicular damage can be prevented by vaccination.
SARS-CoV-2 can cause acute testicular damage with subsequent chronic asymmetric testicular atrophy and associated hormonal changes despite a self-limiting pneumonia in hamsters. Awareness of possible hypogonadism and subfertility is important in managing convalescent coronavirus disease 2019 in men.
严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 在睾丸损伤发病机制中的作用尚不确定。
我们通过鼻内或直接睾丸接种流感病毒 A(H1N1)pdm09 作为对照,研究了野生型 SARS-CoV-2 及其变体感染仓鼠后睾丸的病毒学、病理学和免疫学变化。
除了自限性呼吸道感染外,鼻内 SARS-CoV-2 攻毒还导致感染后 4-7 天精子计数、血清睾酮和抑制素 B 急性下降;感染后 42-120 天睾丸体积和重量以及血清性激素慢性减少。随着病毒接种量的增加,急性组织病理学损伤伴有睾丸炎症、出血、坏死、生精小管变性和有序精子发生破坏程度加重。发现 Sertoli 和 Leydig 细胞变性和死亡。尽管睾丸组织中的病毒载量和 SARS-CoV-2 核衣壳蛋白表达明显低于肺部组织,但 SARS-CoV-2 的直接睾丸内注射显示核衣壳表达间质细胞和附睾上皮细胞,而鼻内或睾丸内接种 A(H1N1)pdm09 对照则没有睾丸感染或损伤。感染后 7-120 天,生精小管变性和凋亡、免疫复合物沉积、生精细胞和精子耗竭持续存在。鼻内攻毒奥密克戎和德尔塔变体也可引起类似的睾丸变化。这种睾丸损伤可以通过疫苗接种来预防。
尽管在仓鼠中 SARS-CoV-2 引起的肺炎呈自限性,但仍可引起急性睾丸损伤,随后出现慢性非对称性睾丸萎缩和相关的激素变化。在管理男性恢复期 2019 冠状病毒病时,需要注意可能发生的性腺功能减退和生育力下降。