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Table 2 Anti-HIV activity of human defensins

From: Host factors influencing susceptibility to HIV infection and AIDS progression

Defensins

Regulation

Cell Source

Mechanisms

References

α-Defensins

    

HNP1, HNP2, and HNP3

Constitutive HPN2 may be the product of proteolytic processing of HNP1/HPN3

Neutrophils and promyelocytes

• CD4 down-modulation

• Viral membrane disruption and binding to CD4 and gp120 (in absence of serum)

• Upregulation of CC-chemokines in macrophages

• Block of nuclear transport (by HNP1)

131, 143, 146

HNP4

Constitutive

Neutrophils

• Unknown (lectin-independent mechanism)

135

β-Defensins

    

HBD2 and HBD3

Inducible by HIV, opportunistic infections, and pro-inflammatory cytokines (TNF, IL-1B)

Epithelial cells, monocytes, monocytes-derived DCs, macrophages, and keratinocytes

• Viral membrane disruption (absence of serum)

• CXCR4 down-modulation

• CCR6-mediated chemotactic effects

148–151

θ-Defensins

    

Retrocyclins (RTD1, RTD2)

Synthesis blocked in humans by premature termination codon

RNA transcripts, not protein, expressed in bone marrow

• Prevent HIV entry by binding to CD4 and gp120

138–140