Volume 7, Issue 4 (Winter 2004)                   J Arak Uni Med Sci 2004, 7(4): 45-50 | Back to browse issues page

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Mosayebi G, Moshfeghi K, Moazzeni M, Shokri F. Designing of A Mixed Elisa Method for Detection of IgM and IgA Rheumatoid Factors. J Arak Uni Med Sci 2004; 7 (4) :45-50
URL: http://jams.arakmu.ac.ir/article-1-6814-en.html
Abstract:   (1148 Views)
Introduction: different  isotypes  of  antibody  can  be  produced  by  immune  system  after  antigen  contact.  Detection  and  measurement  of  different  classes  of  antibody  against  the  antigen  is  very  important  in  some  cases.  The  aim  of  this  study  is  designing  of  an  ELISA  method  on  the  basis  of  inhibition  of  enzyme  activity  by  using  a  non-competitive  inhibitor.  Therefore  in  this  study  rheumatoid  factor  is  used  as  a  model  for  the  detection  of  different  other  classes  of  antibodies  against  the  antigen.
Materials  and  Methods:  In  this  cross  sectional  analytical  study, we  measured  IgM  and IgA   rheumatoid  factors  in  sera  of  10  patients  with  rheumatoid  arthritis  and  positive  latex  test , by  mixed  and  routine  ELISA.  In  mixed  ELISA  the activity  of  the  first  conjugated  enzyme  was  blocked  by  a  non-competitive  inhibitor  after  adding  the  substrate. Then  the  next  conjugated  antibody, which  was  specific  for  another  isotype, was  added. By  optical  density, results  was  comparisoned  with  routine  ELISA.
Results:  The  obtained  results  showed  that  the  average  optical  density  is  lower  when  compared  with  routine  ELISA , but  the  difference  is   not  statistically  significant.  however  these  two  methods  did  not  show  any  significant  difference  in  quantifying  antibody  isotypes. Also  there  is  a  positive  association  between  mixed  and  routine  ELISA (r=0.9, p=0.001).
Discussion: Lower  optical  density  in  mixed  ELISA  is  probably  because  of  stick  hindrance  by  the  first  conjugate. So, because  there  is  no significant  difference  between  the  results  of  these two  types  of  ELISA, and  also  no  need  to  repeat  the  test  for  each  isotype  in  this  method, it  is  recommended  to  use the  new  method  instead  of  the  routine  one  to  save  time  and  reagents.
 
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Subject: General
Received: 2021/01/29 | Accepted: 2004/12/30

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