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Untitled - D Ank Unlimited

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maternal antibodies 482 matrix metalloproteinases (MMPs)<br />

Protein Solution<br />

in Low Concentration<br />

Attachment<br />

to receptors<br />

Microvilli<br />

Phagosome<br />

Lysosome<br />

Fusion and<br />

digestion<br />

Phagolysome<br />

releasing<br />

undigested protein<br />

from cell<br />

membranes. The passively administered antibodies become<br />

bound to the glomerular basement membrane, fix complement,<br />

and induce glomerular basement membrane injury<br />

with increased permeability. Neutrophils and monocytes<br />

may infiltrate the area. Masugi nephritis is an experimental<br />

model of Goodpasture’s syndrome in humans. Also called<br />

nephrotoxic nephritis.<br />

maternal antibodies<br />

Maternal immunoglobulins are passed to offspring both<br />

in utero and in the neonatal period. In humans, immunoglobulin<br />

G (IgG) is transferred by way of the placenta as<br />

early as the 38th day of gestation. Transfer remains stable<br />

until the 17th week and then increases until term. Only the<br />

IgG class of antibodies crosses the placenta. The SC portion<br />

of the immunoglobulin is bound to specific placental<br />

membrane receptors of the Scγ type III variety (CD16) that<br />

possess binding sites for the Foc region of IgG in addition<br />

to epitopes that can be recognized by the antigen-binding<br />

site of IgG. The receptors have low affinity for aggregated<br />

or complex IgG, with the strongest affinity for IgG 1 and<br />

IgG 3, less for IgG 4, and least for IgG 2; they have no affinity<br />

for IgM and IgA. The receptors are concentrated on syncytiotrophoblasts<br />

that make direct contact with the mother’s<br />

circulation. Human colostrum and fresh breast milk contain<br />

numerous specific and nonspecific host resistance factors.<br />

Secretory IgA is present in these fluids, with the highest<br />

concentration in colostrom that peaks during the first<br />

34 days postpartum. Breast-fed children receive 0.5 g of<br />

secretory IgA per day. Human milk also contains IgG and<br />

IgM, as well as secretory IgA but in lower concentrations.<br />

Factors other than immunoglobulins that protect against<br />

infections include lactoferrin that acts as a bacteriostatic<br />

agent depriving microbes of iron. Lysozyme is also present<br />

in milk. Breast milk also contains macrophages, T and B<br />

Protein Solution<br />

in High Concentration<br />

(a) (b)<br />

Maternal antibodies.<br />

Attachment<br />

to receptors<br />

Microvilli<br />

Phagosome<br />

Lysosome<br />

Fusion and<br />

digestion<br />

Phagolysome<br />

releasing<br />

undigested protein<br />

from cell<br />

cells, neutrophils, epithelial cells, and immunomodulators.<br />

Diseases caused by maternal antibodies are listed individually.<br />

Refer also to Brambell receptor.<br />

maternal immunity<br />

Passive immunity conferred on the neonate by its mother.<br />

This is accomplished prepartum by active immunoglobulin<br />

transport across the placenta from the maternal to the fetal<br />

circulation in primate animals including humans. Other<br />

species such as ungulates transfer immunity from mother to<br />

young via antibodies in the colostrum, as the intestine can<br />

pass immunoglobulin molecules across its surface in the<br />

early neonatal period. The egg yolk of avian species is the<br />

mechanism through which immunity is passed from mother<br />

to young.<br />

maternal immunoglobulins<br />

Refer to maternal antibodies.<br />

maternal imprinting<br />

Alteration of the maternal allele chromatin of a gene in<br />

a subject to render it more likely to be expressed than<br />

the paternal allele. Concerns the relationship between a<br />

disease-related allele and the incidence of the disease.<br />

matrix (HIV)<br />

Provides the scaffolding that the viral envelope enfolds.<br />

matrix metalloproteinases (MMPs)<br />

A family of zinc-containing endoproteinases that adjust<br />

specific components of extracellular matrix, thereby<br />

contributing to matrix equilibrium and structural integrity.<br />

They are grouped in three categories: (1) interstitial collagenases,<br />

(2) stromelysins, and (3) gelatinases. Dysregulation<br />

of MMP synthesis and activation is believed to contribute<br />

to tissue injury in inflammatory and neoplastic diseases.<br />

Macrophages, T lymphocytes, eosinophils, and neutrophils<br />

all produce MMPs with cell-specific patterns. MMPs from<br />

macrophages contribute to the degradation, removal, and

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