Progesterone increases susceptibility and decreases immune responses to genital herpes infection

被引:188
作者
Kaushic, C [1 ]
Ashkar, AA [1 ]
Reid, LA [1 ]
Rosenthal, KL [1 ]
机构
[1] McMaster Univ, Ctr Gene Therapeut, Dept Pathol & Mol Med, Ctr Hlth Sci, Hamilton, ON L8N 3Z5, Canada
关键词
D O I
10.1128/JVI.77.8.4558-4565.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Depo-provera, a long-acting progestational formulation, is widely used to facilitate infection of sexually transmitted diseases in animal models. We have previously reported that hormone treatments change susceptibility and immune responses to genital tract infections. In this study we compared the changes in susceptibility of mice to genital herpes simplex virus type 2 (HSV-2) after Depo-provera or a saline suspension of progesterone (P-sal). We found that following Depo-provera-treatment, mice had prolonged diestrus that lasted more than 4 weeks. This coincided with a 100-fold increase in susceptibility to genital HSV-2 compared to that of untreated mice. Mice given P-sal were in diestrous stage for 4 to 6 days before returning to irregular reproductive cycles. When these mice were infected at diestrus they showed a 10-fold increase in susceptibility compared to that of normal, untreated mice. P-sal-treated mice infected at estrus were susceptible to HSV-2, depending on the infectious dose. Normal, untreated mice in estrus were not susceptible to HSV-2, even at a high infectious dose of 10(7) PFU. In addition to alterations in susceptibility, Depo-provera treatment had inhibitory effects on immune responses to HSV-2. Mice immunized with HSV-2 protein (gB) and treated with Depo-provera showed significant lowering of local HSV-2-specific immunoglobulin G (IgG) and IgA in their vaginal washes. Mice immunized with an attenuated strain of HSV-2 2 weeks after Depo-provera treatment failed to develop protection when challenged intravaginally with wild-type HSV-2. In contrast, mice given progesterone and immunized at diestrus or estrus were completely protected from intravaginal challenge. These studies show that Depo-provera treatment changes susceptibility and local immune responses to genital HSV-2 infection. Animal models and vaccine strategies for sexually transmitted diseases need to consider the effect of hormone treatments on susceptibility and immune responses.
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页码:4558 / 4565
页数:8
相关论文
共 23 条
[1]   Long-lived cytotoxic T lymphocyte memory in mucosal tissues after mucosal but not systemic immunization [J].
Gallichan, WS ;
Rosenthal, KL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (05) :1879-1890
[2]   Effects of the estrous cycle on local humoral immune responses and protection of intranasally immunized female mice against herpes simplex virus type 2 infection in the genital tract [J].
Gallichan, WS ;
Rosenthal, KL .
VIROLOGY, 1996, 224 (02) :487-497
[3]   Long-term immunity and protection against herpes simplex virus type 2 in the murine female genital tract after mucosal but not systemic immunization [J].
Gallichan, WS ;
Rosenthal, KL .
JOURNAL OF INFECTIOUS DISEASES, 1998, 177 (05) :1155-1161
[4]   Intranasal immunization with CpG oligodeoxynucleotides as an adjuvant dramatically increases IgA and protection against herpes simplex virus-2 in the genital tract [J].
Gallichan, WS ;
Woolstencroft, RN ;
Guarasci, T ;
McCluskie, MJ ;
Davis, HL ;
Rosenthal, KL .
JOURNAL OF IMMUNOLOGY, 2001, 166 (05) :3451-3457
[5]  
Kaushic C, 1998, AM J REPROD IMMUNOL, V39, P209
[6]   REGULATION OF POLYMERIC IMMUNOGLOBULIN-A RECEPTOR MESSENGER-RIBONUCLEIC-ACID EXPRESSION IN RODENT UTERI - EFFECT OF SEX-HORMONES [J].
KAUSHIC, C ;
RICHARDSON, JM ;
WIRA, CR .
ENDOCRINOLOGY, 1995, 136 (07) :2836-2844
[7]   Effects of estradiol and progesterone on susceptibility and early immune responses to Chlamydia trachomatis infection in the female reproductive tract [J].
Kaushic, C ;
Zhou, F ;
Murdin, AD ;
Wira, CR .
INFECTION AND IMMUNITY, 2000, 68 (07) :4207-4216
[8]   Polymeric immunoglobulin A receptor in the rodent female reproductive tract: Influence of estradiol in the vagina and differential expression of messenger ribonucleic acid during estrous cycle [J].
Kaushic, C ;
Frauendorf, E ;
Wira, CR .
BIOLOGY OF REPRODUCTION, 1997, 57 (05) :958-966
[9]  
Kuklin NA, 1998, J IMMUNOL, V160, P5998
[10]   IGA AND MUCOSAL DEFENSE [J].
LAMM, ME ;
NEDRUD, JG ;
KAETZEL, CS ;
MAZANEC, MB .
APMIS, 1995, 103 (04) :241-246