期刊论文详细信息
European Journal of Medical Research
An immunohistochemical study of CD83- and CD1a-positive dendritic cells in the decidua of women with recurrent spontaneous abortion
Xiao-Ming Zhu1  Li-Li Huang2  Zhi-Da Qian2 
[1] Key Laboratory of Reproductive Genetics (Zhejiang University), Ministry of Education, Hangzhou, People’s Republic of China;Department of Obstetrics and Gynecology, Women’s Hospital, School of Medicine, Zhejiang University, 1 Xueshi Road, Hangzhou 310006, Zhejiang Province, People’s Republic of China
关键词: immunohistochemistry;    CD1a;    CD83;    dendritic cells;    decidua;    recurrent spontaneous abortion;   
Others  :  1103403
DOI  :  10.1186/s40001-014-0076-2
 received in 2014-01-20, accepted in 2014-12-08,  发布年份 2015
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【 摘 要 】

Background

There are more and more women with recurrent spontaneous abortion (RSA). The mechanism of RSA is still unclear. Immunological factors have been postulated to play a role in the etiology of RSA. Dendritic cells (DCs) are the most potent antigen-presenting cells in the immune system, and the decidual DCs may take part in the occurrence of RSA. The difference in maturity status of decidual DCs among women with RSA and women with normal pregnancies is worthy of studying for its application to prevention and therapy.

Methods

The EnVision two-step immunohistochemical staining technique was used to detect the expression of CD83 and CD1a in the decidua of women with RSA (30 cases) and normal pregnancies (30 cases). The maturity status, distribution and quantity of DCs in the two groups were observed. Observation of the staining and cell counting were done using microscope within 30 randomly selected high-power fields (HPF, 40 × 10). All data analyses were conducted with SPSS 17.0 and the statistical significance was set at P <0.05.

Results

The decidua from the two groups contained DCs that stained with the anti-CD83 and anti-CD1a antibody. Most of the decidual CD83+DCs from two groups were located in the stroma. There were more CD83+DCs clustered with other DCs in the stroma from women with RSA than normal pregnancies. Most of the CD1a+DCs in the decidua from the two groups are located close to maternal glandular epithelium. No difference in the location of CD1a+DCs was found in the decidua between two groups. The number of decidual CD83+DCs was statistically significantly higher in RSA women than in normal early pregnant women (14.20 ± 13.34/30 HPF versus 4.77 ± 2.64/30 HPF; t = 3.800, P = 0.001). The number of CD1a+DCs in the decidua was statistically significantly lower in RSA women compared with normal early pregnant women (3.97 ± 3.75/30 HPF versus 7.60 ± 6.08/30 HPF; t = 2.786, P = 0.008).

Conclusions

These findings suggest that the increase in the number of mature DCs and the decrease in the quantity of immature DCs in the decidua may be related to RSA. The maturation of decidual DCs may play an important role in the pathogenesis of RSA.

【 授权许可】

   
2014 Qian et al.; licensee BioMed Central.

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【 参考文献 】
  • [1]Rai R, Regan L: Recurrent miscarriage. Lancet 2006, 368:601-611.
  • [2]Blois S, Alba Soto CD, Olmos S, Chuluyan E, Gentile T, Arck PC, Margni RA: Therapy with dendritic cells influences the spontaneous resorption rate in the CBA/J x DBA/2 J mouse model. Am J Reprod Immunol 2004, 51:40-48.
  • [3]Kammerer U: Antigen-presenting cells in the decidua. Chem Immunol Allerg 2005, 89:96-104.
  • [4]Sanguansermsri D, Pongcharoen S: Pregnancy immunology: decidual immune cells. Asian Pac J Allergy Immunol 2008, 26:171-181.
  • [5]Steinman RM: The dendritic cell system and its role in immunogenicity. Annu Rev Immunol 1991, 9:271-296.
  • [6]Banchereau J, Steinman RM: Dendritic cells and the control of immunity. Nature 1998, 392:245-252.
  • [7]Banchereau J, Briere F, Caux C, Davoust J, Lebecque S, Liu YJ, Pulendran B, Palucka K: Immunobiology of dendritic cells. Annu Rev Immunol 2000, 18:767-811.
  • [8]Chorny A, Gonzalez-Rey E, Delgado M: Regulation of dendritic cell differentiation by vasoactive intestinal peptide: therapeutic applications on autoimmunity and transplantation. Ann NY Acad Sci 2006, 1088:187-194.
  • [9]Reid DC: Dendritic cells and immunotherapy for malignant cells. Br J Haematol 2001, 112:874-875.
  • [10]Abraham S, Indrasingh I, Vettivel S, Chandi G: Gross morphology and ultrastructure of dendritic cells in the normal human decidua. Clin Anat 2000, 13:177-180.
  • [11]Prechtel AT, Steinkasserer A: CD83: an update on functions and prospects of the maturation marker of dendritic cells. Arch Dermatol Res 2007, 299:59-69.
  • [12]Coventry BJ, Austyn JM, Chryssidis S, Hankins D, Harris A: Identification and isolation of CD1a positive putative tumour infiltrating dendritic cells in human breast cancer. Adv Exp Med Biol 1997, 417:571-577.
  • [13]Gardner L, Moffett A: Dendritic cells in the human decidua. Biol Reprod 2003, 69:1438-1446.
  • [14]von Bergwelt-Baildon MS, Popov A, Saric T, Chemnitz J, Classen S, Stoffel MS, Fiore F, Roth U, Beyer M, Debey S, Wickenhauser C, Hanisch FG, Schultze JL: CD25 and indoleamine 2,3-dioxygenase are up-regulated by prostaglandin E2 and expressed by tumor-associated dendritic cells in vivo: additional mechanisms of T-cell inhibition. Blood 2006, 108:228-237.
  • [15]Koya T, Matsuda H, Takeda K, Matsubara S, Miyahara N, Balhorn A, Dakhama A, Gelfand EW: IL-10-treated dendritic cells decrease airway hyperresponsiveness and airway inflammation in mice. J Allergy Clin Immunol 2007, 119:1241-1250.
  • [16]Khanna A, Morelli AE, Zhong C, Takayama T, Lu L, Thomson AW: Effects of liver-derived dendritic cell progenitors on Th1-and Th2-like cytokine responses in vitro and in vivo. J Immunol 2000, 164:1346-1354.
  • [17]Blois SM, Barrientos G, Garcia MG, Orsal AS, Tometten M, Cordo-Russo RI, Klapp BF, Santoni A, Fernández N, Terness P, Arck PC: Interaction between dendritic cells and natural killer cells during pregnancy in mice. J Mol Med 2008, 86:837-852.
  • [18]Miranda S, Litwin S, Barrientos G, Szereday L, Chuluyan E, Bartho JS, Arck PC, Blois SM: Dendritic cells therapy confers a protective microenvironment in murine pregnancy. Scand J Immunol 2006, 64:493-499.
  • [19]Askelund K, Liddell HS, Zanderigo AM, Fernando NS, Khong TY, Stone PR, Chamley LW: CD83(+) dendritic cells in the decidua of women with recurrent miscarriage and normal pregnancy. Placenta 2004, 25:140-145.
  • [20]Kämmerer U, Schoppet M, McLellan AD, Kapp M, Huppertz HI, Kämpgen E, Dietl J: Human decidua contains potent immunostimulatory CD83(+) dendritic cells. Am J Pathol 2000, 157:159-169.
  • [21]Dealtry GB, O’Farrell MK, Fernandez N: The Th2 cytokine environment of the placenta. Int Arch Allergy Immunol 2000, 123:107-119.
  • [22]Chaouat G, Ledee-Bataille N, Dubanchet S, Zourbas S, Sandra O, Martal J: TH1/TH2 paradigm in pregnancy: paradigm lost? Cytokines in pregnancy/early abortion: reexamining the TH1/TH2 paradigm. Int Arch Allergy Immunol 2004, 134:93-119.
  • [23]Cools N, Van Tendeloo VF, Smits EL, Lenjou M, Nijs G, Van Bockstaele DR, Berneman ZN, Ponsaerts P: Immuno-suppression induced by immature dendritic cells is mediated by TGF-beta/IL-10 double - positive CD4 + regulatory T cells. J Cell Mol Med 2008, 12:690-700.
  • [24]Encabo A, Solves P, Carbonell-Uberos F, Minana MD: The functional immaturity of dendritic cells can be relevant to increased tolerance associated with cord blood transplantation. Transfusion 2007, 47:272-279.
  • [25]Blois SM, Alba Soto CD, Tometten M, Klapp BF, Margni RA, Arck PC: Lineage, maturity, and phenotype of uterine murine dendritic cells throughout gestation indicate a protective role in maintaining pregnancy. Biol Reprod 2004, 70:1018-1023.
  • [26]Miwa N, Hayakawa S, Miyazaki S, Myojo S, Sasaki Y, Sakai M, Takikawa O, Saito S: IDO expression on decidual and peripheral blood dendritic cells and monocytes/macrophages after treatment with CTLA-4 or interferon-γ increase in normal pregnancy but decrease in spontaneous abortion. Mol Hum Reprod 2005, 11:865-870.
  • [27]Ban YL, Kong BH, Qu X, Yang QF, Ma YY: BDCA-1+, BDCA-2+ and BDCA-3+ dendritic cells in early human pregnancy decidua. Clin Exp Immunol 2008, 151:399-406.
  • [28]Kammerer U, Kruse A, Barrientos G, Arck PC, Blois SM: Role of dendritic cells in the regulation of maternal immune responses to the fetus during mammalian gestation. Immunol Invest 2008, 37:499-533.
  • [29]Zenclussen AC: CD4 + CD25+ regulatory T cells in murine pregnancy. J Reprod Immunol 2005, 65:101-110.
  • [30]Somerset DA, Zheng Y, Kilby MD, Sansom DM, Drayson MT: Normal human pregnancy is associated with an elevation in the immune suppressive CD25 + CD4+ regulatory T-cell subset. Immunology 2004, 112:38-43.
  • [31]Mei S, Tan J, Chen H, Chen Y, Zhang J: Changes of CD4 + CD25 high regulatory T cells and FOXP3 expression in unexplained recurrent spontaneous abortion patients. Fertil Steril 2010, 94:2244-2247.
  • [32]Savina A, Jancic C, Hugues S, Guermonprez P, Vargas P, Moura IC, Lennon-Duménil AM, Seabra MC, Raposo G, Amigorena S: NOX2 controls phagosomal PH to regulate antigen processing during crosspresentation by dendritic cells. Cell 2006, 126:205-218.
  • [33]Misra N, Bayry J, Lacroix-Desmazes S, Kazatchkine MD, Kaveri SV: Cutting edge human CD4 + CD25+ T cells restrain the maturation and antigen-presenting function of dendritic cells. J Immunol 2004, 172:4676-4680.
  • [34]Zhang BY, Wei YS, Niu JM, Li Y, Miao ZL, Wang ZN: Risk factors for unexplained recurrent spontaneous abortion in a population from southern China. Int J Gynaecol Obstet 2010, 108:135-138.
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