Mucosal sites have an innate defense system-which includes immune cells, an
tibodies, and mucus-to protect the body from opportunistic pathogens. Some
sexually transmitted diseases (STDs), such as HIV, utilize host defense mec
hanisms to evade detection by infecting motile immune cells present at the
site. The infected cells migrate through the mucus layer and penetrate the
epithelium undetected. A new strategy for preventing STDs could involve inh
ibiting cell migration through the mucus. One method for inhibiting migrati
on is to alter the barrier property of mucus by modifying its gel structure
. Mucin, the structural component of mucus, is a high molecular weight anio
nic molecule, which forms an entangled fiber network through non-covalent i
nteractions. The addition of nonionic or cationic polymers, such as poly(et
hylene glycol) (PEG) or poly(vinyl pyridine) (PVP), altered the overall gel
structure as revealed by scanning electron microscopy (SEM), while anionic
poly(acrylic acid) had little effect on the structure. Acid residues on mu
cin associate with PEG through hydrogen bonds to form regions of coalesced
fibers within the mucus. PVP, however, interacts with mucin via electrostat
ic bonds, forming a gel that had areas of aggregated fibers adjacent to reg
ions with virtually no fibers. These results suggest that addition of small
amounts of certain synthetic polymers will modify mucus structure; these c
hanges should alter the barrier properties of mucus. (C) 2001 Elsevier Scie
nce Ltd. All rights reserved.