New concepts in regenerative medicine approaches to the treatment of female stress urinary incontinence

被引:20
作者
Bennington, Julie [1 ]
Williams, James Koudy [1 ]
Andersson, Karl-Erik [1 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Inst Regenerat Med, Richard H Dean Biomed Bldg,391 Technol Way, Winston Salem, NC 27101 USA
关键词
animal models; chemokines; chronic intrinsic sphincter deficiency; noncell-based treatments; NONHUMAN PRIMATE MODEL; CELL THERAPY; HOMING FACTOR; FACTOR-I; MUSCLE; MANAGEMENT; CCL7;
D O I
10.1097/MOU.0000000000000617
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Update on recent regenerative medicine approaches to the treatment of stress urinary incontinence (SUI) caused by intrinsic sphincter deficiency (ISD). Recent findings In the treatment of female SUI/ ISD, results using different types of cellular therapy have been disappointing, and new approaches are desirable. To advance our regenerative medicine approaches to SUI/ ISD, it is critical to utilize animal models that best parallel the pathophysiology of this disease in women. Many current animal models mimic acute SUI/ ISD. However, SUI/ ISD in women is usually a chronic condition resulting from previous muscle and nerve sphincter damage during parturition or muscle loss during aging. Similar to women, a nonhuman primate (NHP) model of chronic SUI/ ISD has demonstrated only modest response to cell therapy. However, treatment with stromal cell-derived factor 1 (SDF1), also known as C-X-C motif chemokine 12 (CXCL12) restored continence in this model. Summary As a potential therapeutic approach, the use of a well characterized chemokine, such as CXCL12, may bypass the lengthy and expensive process of cell isolation, expansion, and injection. Recent findings in this new NHP model of chronic SUI/ ISD may open up the field for noncell-based treatments.
引用
收藏
页码:380 / 384
页数:5
相关论文
共 36 条
[1]  
Abrams P., 2017, INCONTINENCE, V2 vol
[2]   Long-Term Structural and Functional Effects of Autologous Muscle Precursor Cell Therapy in a Nonhuman Primate Model of Urinary Sphincter Deficiency [J].
Badra, Sherif ;
Andersson, Karl-Erik ;
Dean, Ashley ;
Mourad, Sherif ;
Williams, J. Koudy .
JOURNAL OF UROLOGY, 2013, 190 (05) :1938-1945
[3]   A Nonhuman Primate Model of Stable Urinary Sphincter Deficiency [J].
Badra, Sherif ;
Andersson, Karl-Erik ;
Dean, Ashley ;
Mourad, Sherif ;
Williams, J. Koudy .
JOURNAL OF UROLOGY, 2013, 189 (05) :1967-1974
[4]   Prevalence of Female Urinary Incontinence in the General Population According to Different Definitions and Study Designs [J].
Bedretdinova, Dina ;
Fritel, Xavier ;
Panjo, Henri ;
Ringa, Virginie .
EUROPEAN UROLOGY, 2016, 69 (02) :256-264
[5]  
BUNNE G, 1978, UROL RES, V6, P127
[6]   Microparticles: biomarkers and beyond [J].
Burger, Dylan ;
Schock, Sarah ;
Thompson, Charlie S. ;
Montezano, Augusto C. ;
Hakim, Antoine M. ;
Touyz, Rhian M. .
CLINICAL SCIENCE, 2013, 124 (7-8) :423-441
[7]   Intrapartum predictors of maternal levator ani injury [J].
Caudwell-Hall, Jessica ;
Atan, Ixora Kamisan ;
Martin, Andrew ;
Rojas, Rodrigo Guzman ;
Langer, Susanne ;
Shek, Kalai ;
Dietz, Hans P. .
ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA, 2017, 96 (04) :426-431
[8]   Longitudinal follow-up of levator ani muscle avulsion: does a second delivery affect it? [J].
Chan, S. S. C. ;
Cheung, R. Y. K. ;
Lee, L. L. ;
Choy, R. K. W. ;
Chung, T. K. H. .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2017, 50 (01) :110-115
[9]   The role of CXCL12 and CCL7 chemokines in immune regulation, embryonic development, and tissue regeneration [J].
Cheng, Julie W. ;
Sadeghi, Zhina ;
Levine, Alan D. ;
Penn, Marc S. ;
von Recum, Horst A. ;
Caplan, Arnold I. ;
Hijaz, Adonis .
CYTOKINE, 2014, 69 (02) :277-283
[10]   Extracellular vesicles: potential roles in regenerative medicine [J].
De Jong, Olivier G. ;
Van Balkom, Bas W. M. ;
Schiffelere, Raymond M. ;
Bouten, Carlijn V. C. ;
Verhaar, Marianne C. .
FRONTIERS IN IMMUNOLOGY, 2014, 5 :1-13