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. 2023 Feb 17;11(2):519. doi: 10.3390/microorganisms11020519

Table 2.

Comparison of ELISAs for detecting anti-VZV antibodies.

Type Characteristics Advantages Limitations
WC-ELISA Using whole lysates of VZV-infected cells as antigens
  • Commercially available.

  • Antibodies against all VZV antigens can be detected.

  • Not sensitive enough to measure antibody responses to chickenpox vaccination.

gp-ELISA Using purified VZV glycoproteins as antigens
  • Commercially available.

  • Higher sensitivity and specificity than WC-ELISA.

  • Not sensitive enough to measure antibody responses to chickenpox vaccination (expect the Merck gp-ELISA).

  • High cost of glycoprotein purification.

gE-ELISA Using purified VZV gE as an antigen
  • Higher sensitivity and specificity than WC-ELISA.

  • Not commercially available.

  • Only test for anti-gE antibodies.

Double antibody sandwich competitive ELISA Capture antibody: anti-ORF9 antibody
Detection antibody:
HRP-labeled anti-gE antibody
  • Comparable sensitivity and specificity to FAMA

  • Not commercially available.

  • Lacking further validation.

Double gE antigen sandwich ELISA Using purified VZV gE as the coating antigen and HRP-labeled gE as the detection antigen.
  • Comparable sensitivity and specificity to FAMA

  • Not commercially available.

  • Lacking further validation.