14,20 In many HIV-infected

women, the plasma viral load (PVL) has not been found to correlate with genital tract viral load (GTVL) and has also been found to be genetically distinct.21–23 Genital tract viral shedding can be highly localized and can change with the menstrual cycle (S. Cu-Uvin, unpublished data,24,25). In addition, the proportion of virus in the genital tract that is actually infectious and capable of transmission seems to be very low, irrespective of the PVL and the GTVL (M. Ghosh and J. V. Fahey, unpublished data;26,27). In a study by Keller et al.,14 the CVL was collected from normal women throughout the course of the menstrual cycle and assayed for a number of immune activators, antimicrobials and antibodies. CVL samples were found Selleckchem PF-562271 to contain a spectrum of factors, most of which changed with the menstrual cycle, specifically dipping

at mid-cycle to the early secretory phase, which has been proposed as a ‘window of vulnerability’ through which women become infected with HIV.28 Many of the innate immune molecules that are known to protect the FRT18,19,29 are regulated by the sex selleck chemicals hormones oestradiol and progesterone during the menstrual cycle.30–32 Two such molecules are the anti-proteases secretory leucocyte protease inhibitor (SLPI) and Trappin-2/Elafin. SLPI and Trappin-2/Elafin are members of the whey acidic protein (WAP) family. They are produced by multiple cell types, secreted in mucosal secretions constitutively and can be elevated in the presence of inflammatory stimuli.33–37 These molecules are anti-inflammatory; they function by inhibiting specific neutrophil proteases. Trappin-2/Elafin has been demonstrated to inhibit neutrophil Acesulfame Potassium elastase and proteinase 3.19 In addition, both SLPI and Trappin-2/Elafin have been demonstrated to have antimicrobial activity.38–41 The main mechanism for this activity is predicted to be the cationic nature of these molecules, which destabilizes the negative charges of the bacterial cell wall or the viral envelope.40,41 Trappin-2/Elafin

has specifically been shown to have antimicrobial activity against both Gram-positive and Gram-negative bacteria, and fungi.39 Trappin-2/Elafin is unique in that it can be biologically active as both cell-associated and secreted protein. The precursor of Trappin-2/Elafin is known as Trappin-2, which contains a transglutaminase substrate-binding domain (TSBD) that is cleaved from the processed Trappin-2/Elafin molecule. The TSBD is involved in covalent binding to extracellular matrix proteins, including laminin, fibronectin, collagen IV, elastin and fibrinogen.33,40 This might provide local protection from proteolytic activity by endogenous proteases, whereas the cleaved soluble form can act at distant sites. Trappin-2/Elafin has been found to be involved in immune disorders of the skin, such as psoriasis42 and lung chronic obstructive pulmonary disorder (COPD43).