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in vitro culture and isoenzyme analysis of giardia lamblia

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two factors are associated with the development <strong>of</strong> symptoms, namely the degree<br />

<strong>of</strong> <strong>in</strong>flammatory changes <strong>in</strong> the small bowel <strong>and</strong> damage to microvilli, which lead to<br />

a deficiency <strong>of</strong> brush border enzymes, particularly lactase.<br />

1.5.2 Do host factors play a role <strong>in</strong> <strong>in</strong>creas<strong>in</strong>g the susceptibility <strong>of</strong> certa<strong>in</strong><br />

hosts to <strong>in</strong>fection?<br />

Many variables such as age, sex, immune <strong>and</strong> nutritional status, ABO blood<br />

groups, Human Leukocyte Antigen (HLA) type, socio-economic factors <strong>and</strong> gastric<br />

acidity have been implicated <strong>in</strong> predispos<strong>in</strong>g hosts to <strong>giardia</strong>sis. The exact nature<br />

<strong>of</strong> the relationship between 'the disease <strong>and</strong> these factors has not been<br />

conclusively described. Brief discussions on these factors are outl<strong>in</strong>ed <strong>in</strong> 1.7<br />

below.<br />

1.5.3 Are immune responses elicited by <strong>in</strong>fection with Giardia responsible<br />

for parasite clearance <strong>and</strong> sterilis<strong>in</strong>g immunity?<br />

In some <strong>in</strong>stances these <strong>in</strong>fections are cleared spontaneously. However re<strong>in</strong>fection<br />

<strong>of</strong> hosts frequently occurs (Farth<strong>in</strong>g et al., 1986; Gilman et al., 1988). It is<br />

not clear whether partial protective humoral immunity occurs <strong>in</strong> <strong>giardia</strong>sis. Re<strong>in</strong>fection<br />

has been documented <strong>in</strong> <strong>in</strong>fants <strong>and</strong> children (Farth<strong>in</strong>g et al., 1986) as<br />

well as <strong>in</strong> adults (Nash et al., 1987; Gilman et al., 1988), thus the issue <strong>of</strong><br />

immunological maturation with age cannot be used to expla<strong>in</strong> the recurrent<br />

<strong>in</strong>fections <strong>in</strong> some <strong>in</strong>dividuals. In experimental human <strong>in</strong>fections, re-<strong>in</strong>fection was<br />

confirmed as the volunteers were successfully treated after <strong>in</strong>itial <strong>in</strong>fections <strong>and</strong><br />

they were successfully re-challenged (Nash et al., 1987). In stUdies <strong>of</strong> the Giardiaspecific<br />

immune response <strong>in</strong> <strong>in</strong>fected human volunteers, serum immunoglobul<strong>in</strong>s<br />

19

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