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INVITED COMMENTARY
Year : 2016  |  Volume : 18  |  Issue : 3  |  Page : 364

Stem cells, gene therapy, and advanced medical management hold promise in the treatment of male infertility


1 University of Virginia, Department of Urology, Charlottesville, VA 22908, USA
2 Scott Department of Urology, Baylor College of Medicine, Houston, Texas 77030, USA
3 Men's Health Center, 8240 Naab Road, Suite 220, Indianapolis, Indiana 46260, USA

Date of Web Publication08-Apr-2016

Correspondence Address:
Dr. Jason R Kovac
Men's Health Center, 8240 Naab Road, Suite 220, Indianapolis, Indiana 46260
USA
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/1008-682X.179249

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How to cite this article:
Smith RP, Lipshultz LI, Kovac JR. Stem cells, gene therapy, and advanced medical management hold promise in the treatment of male infertility. Asian J Androl 2016;18:364

How to cite this URL:
Smith RP, Lipshultz LI, Kovac JR. Stem cells, gene therapy, and advanced medical management hold promise in the treatment of male infertility. Asian J Androl [serial online] 2016 [cited 2020 Nov 26];18:364. Available from: https://www.ajandrology.com/text.asp?2016/18/3/364/179249 - DOI: 10.4103/1008-682X.179249

Medical management of male infertility has traditionally involved therapies directed toward manipulation of the hypothalamic-pituitary-gonadal axis. The medications available currently are essentially identical to those utilized decades ago. Moreover, these agents require that the infertile patient can produce at least a small number of functional sperm. As conveyed by Dr. Ring et al. [1] in the accompanying manuscript, a significant percentage of male infertility is defined as "idiopathic" suggesting a specific diagnosis was impossible. Moreover, given that a subset of these patients is postulated to have unrecognized genetic etiologies, the notion of targeted medical treatment becomes even more problematic. Many patients are thus placed on empiric therapy in hopes of augmenting baseline spermatogenic function. While this may prove fruitful in patients with intact spermatogenesis, the true challenge lies in the treatment of the azoospermic patient due to testicular failure.

Technologies have emerged in the last decades that hold promise. Given the limitations reported with the currently available empiric medical therapy, there is a clear need for research advances. Some areas that seem poised for such growth include stem cell biology and gene therapy. Indeed, the potential for stem cells to restore fertility following chemotherapy/radiation in men with cancer has been gaining momentum. Brinster and colleagues, in 1994, reported on successful transplantation of mouse spermatogonial stem cells into the seminiferous tubules of infertile recipient mice. [2] This research led to donor-derived spermatogenesis and subsequent paternity. [2] Since then, others have focused on development, proliferation, and differentiation of mature sperm in vitro. The human application requires cryopreservation of tissues before gonadotoxic therapies or, alternatively, harvesting of stem cells from other somatic tissues. Given that there have been reports of in vitro propagation of human prepubertal somatic stem cells, these goals do not seem impossible to obtain. [3] Coupled with the fact that testicular tissue is being obtained and cryopreserved under experimental protocols from prepubertal patients preparing to undergo gonadotoxic therapy, the potential use of this type of therapeutic modality may soon become reality.

Given that many men present with as yet-to-be-identified genetic defects, the notion of gene therapy holds high hopes. Such a treatment would theoretically be able to deliver absent/altered downstream genetic products to complete the cycle of spermatogenesis. A simple example of successful genetic manipulation can be seen in the use of viral vectors to create transgenic animals, [4] thus proving the technology exists. Obviously, caution is warranted since genetic perturbations in humans could result in unintended consequences for both offspring and the patient themselves.

Perhaps an untapped resource in the medical management of male infertility lies in the use of growth hormone (GH). GH receptors have been identified throughout the male reproductive tract and IGF-1 receptors are found in secondary spermatocytes and spermatids. [5] There is currently a paucity of research on the effects of GH supplementation in infertile patients. While GH may have an important physiologic role in spermatogenesis, more studies are needed to define the role of GH therapy in clinical practice.

 
  References Top

1.
Ring JD, Lwin AA, Köhler TS. Recent advancements in the study of male reproduction current medical management of male infertility. Asian J Androl 2016; 18: 357-63.  [Doi: 10.4103/1008-682X.179252] [Epub ahead of print].  Back to cited text no. 1
    
2.
Brinster RL, Zimmermann JW. Spermatogenesis following male germ-cell transplantation. Proc Nat Acad Sci U S A 1994; 91: 11298-302.  Back to cited text no. 2
    
3.
Long CJ, Ginsberg JP, Kolon TF. Fertility preservation in children and adolescents with cancer. Urology 2016. [Doi: 10.1016/j.urology.2015.10.047] [Epub ahead of print].  Back to cited text no. 3
    
4.
Gassei K, Orwig KE. Experimental methods to preserve male fertility and treat male factor infertility. Fertil Steril 2016; 105: 256-66.  Back to cited text no. 4
    
5.
Harvey S, Baudet ML, Murphy A, Luna M, Hull KL, et al. Testicular growth hormone (GH): GH expression in spermatogonia and primary spermatocytes. Gen Comp Endocrinol 2004; 139: 158-67.  Back to cited text no. 5
    



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Current Molecular Medicine. 2019; 19(8): 539
[Pubmed] | [DOI]



 

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