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Antigen: The CF antigen is prepared by GenBio and standardized using ImmunoWELL IgM units. Specimens: Fourteen hundred twenty-six (1426) sera collected from potential U.S. blood donors during 2010 and 2011 are tested. The specimens are collected in thirteen states by Interstate Blood Bank, Memphis, TN, USA. ImmunoWELL: GenBio tested approximately eighty specimens every one to two weeks using ImmunoWELL Mycoplasma Pneumoniae IgM Test following package insert instructions. ImmunoFLOW: ImmunoFLOW Mycoplasma, a flow-through rapid test method, uses this same CF antigen and its clinical cutoff is calibrated using the above standards. A small study conducted by an outside European laboratory tested eighteen (18) specimens using ImmunoCard (Meridian Diagnostics) and ImmunoFLOW following respective package insert instructions. Abstract Mycoplasma pneumoniae is the causative agent of atypical pneumonia. Serological diagnosis detecting antibodies to either an immunodominant membrane protein or the complement fixing lipid antigen is often used. These Mycoplasma antibodies are cross- reactive with other Mycoplasma pneumoniae species, so clinical interpretation is made using a clinical cutoff. The clinical cutoff of ImmunoWELL™ Mycoplasma Pneumoniae IgM Test, using a purified CF antigen, is evaluated using presumptively healthy U.S. blood donors. Materials and Methods: Fourteen hundred twenty-six (1426) sera collected from potential U.S. blood donors collected at centers located in thirteen states is tested. Tests are performed using ImmunoWELL Mycoplasma IgM Test following package insert instructions. Results: Figure 1 illustrates specific antibody distribution in a U.S. healthy, adult population. Summary: The 95 th percentile (736 to 917 units/mL)is consistency with ImmunoWELL’s 950 units/mL clinical cutoff. The 75 th percentile is 295-319 units/mL. Figure 1 Introduction Mycoplasma pneumoniae is the causative agent of atypical pneumonia. Sero-diagnosis detects antibodies against either an immunodominant membrane protein or complement fixing (CF) lipid antigens. Because the membrane protein is water soluble and the CF lipid is not water soluble, only one immune reaction type is detected by most assay methods. Additionally, some older serology kits report analytic results (“epidemiological results”) while newer kits are required to report a clinical cutoff. In the 1980’s, Dr. Stig Jeansson developed an enzyme immunoassay (EIA) method detecting anti-CF. ImmunoWELL (unpublished method). Mycoplasma Pneumoniae IgM Test uses this original design and more recently ImmunoFLOW Mycoplasma Pneumoniae IgM Test also uses the antigen. Originally, the ImmunoWELL™ Mycoplasma Pneumoniae IgM Test’s clinical cutoff was established using healthy U.S. Methods & Materials Figure 1 illustrates anti-CF distribution measured using ImmunoWELL Mycoplasma Pneumoniae IgM Test in a presumptively healthy U.S. adult population. Conclusions These results are substantially the same as originally observed (1996) to establish the kit’s clinical cutoff. Using standards defined using th3 IgM semi- quantitative test, a rapid qualitative test using the same M. pneumoniae CF antigen yields correlative results to an alternative qualitative test. Contact Information Bryan Kiehl ([email protected] ) Mobile (+1 760-855-8999) Frequency of Mycoplasma pneumoniae Complement Fixation IgM in a Healthy, Adult Population B. Kiehl 1 and S. Jeansson 2 1 GenBio, San Diego, 2 Oslo University Hospital, Oslo, Norway Table 1 shows Mycoplasma IgM test results of eighteen clinical specimens using ImmunoCard and ImmunoFLOW, a flow-through test method using the same Mycoplasma pneumoniae CF antigen. Note: ImmunoFLOW is not available within the U.S.; however it is available in the European Union (CE Mark) and other international markets. Results Number of Specimens ImmunoCar d ImmunoFLO W 5 Positive Positive 13 Negative Negative Summary Mycoplasma pneumoniae specific antibody is detected in healthy subjects, presumably because of surface antigen cross-reactivity between Mycoplasma species. Prior to commercial test kits with clinical cutoffs defined by prospective clinical study, acute and convalescent sera (“serum pair”) was required for clinical interpretation. A statistical difference between the specimens is used to aid disease diagnosis. To assure specificity, kits with a clinical cutoff (opposed to the analytic cutoff or older kits) are set at a much higher antibody threshold. This study measures specific IgM in a presumptively healthy population using the semi- quantitative test ImmunoWELL Mycoplasma Pneumoniae IgM. This test detects specific IgM units/m reporting values above 200 units/mL; however, the clinical cutoff is 950 units/mL. Although presumptively healthy U.S. blood donor adult population is not the intended test population, it is easily tested and used by the manufacturer as a means to assure product performance clinical cutoff consistency. During the initial 1996 ImmunoWELL prospective validation study a similar U.S. blood donor population was tested and reported as expected results. The current study results are more extensive and report substantially the same results. Table 2 shows the percentile rankings, corresponding to results. The 95-percentile ranking is 807 units/mL (736 to 917 units/mL) which is consistent with ImmunoWELL’s clinical cutoff. It was also shown that by using ImmunoWELL’s semi-quantitative Percen tile Valu e 95% LCL 95% UCL 99 1458 1226 1699 95 807 736 917 90 607 559 650 85 477 435 528 80 387 361 415 75 319 295 349 70 272 250 293 65 234 217 248 60 199 188 217 55 177 165 190 50 156 142 166 45 132 123 143 40 115 106 124 35 98 90 106 30 82 77 90 25 70 63 76 20 56 52 61 15 44 40 49 10 29 24 36 5 6 0 14 1 0 0 0 Table 2: Percentile Rank of U.S. healthy adult population expressed in IgM Units Table 2: ImmunoCard and ImmunoFLOW Comparison Figure 1: M. pneumoniae IgM Distribution in U.S. Healthy Adult Population

Antigen: The CF antigen is prepared by GenBio and standardized using ImmunoWELL IgM units

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Frequency of Mycoplasma pneumoniae Complement Fixation IgM in a Healthy, Adult Population. B. Kiehl 1 and S. Jeansson 2 1 GenBio, San Diego, 2 Oslo University Hospital, Oslo, Norway. Abstract. Summary. Table 2: Percentile Rank of U.S. healthy adult population expressed in IgM Units. - PowerPoint PPT Presentation

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Page 1: Antigen:  The CF antigen is prepared by GenBio and standardized using ImmunoWELL IgM units

Antigen: The CF antigen is prepared by GenBio and standardized using ImmunoWELL IgM units.Specimens: Fourteen hundred twenty-six (1426) sera collected from potential U.S. blood donors during 2010 and 2011 are tested. The specimens are collected in thirteen states by Interstate Blood Bank, Memphis, TN, USA.ImmunoWELL: GenBio tested approximately eighty specimens every one to two weeks using ImmunoWELL Mycoplasma Pneumoniae IgM Test following package insert instructions.ImmunoFLOW: ImmunoFLOW Mycoplasma, a flow-through rapid test method, uses this same CF antigen and its clinical cutoff is calibrated using the above standards. A small study conducted by an outside European laboratory tested eighteen (18) specimens using ImmunoCard (Meridian Diagnostics) and ImmunoFLOW following respective package insert instructions.

AbstractMycoplasma pneumoniae is the causative agent of atypical pneumonia. Serological diagnosis detecting antibodies to either an immunodominant membrane protein or the complement fixing lipid antigen is often used. These Mycoplasma antibodies are cross-reactive with other Mycoplasma pneumoniae species, so clinical interpretation is made using a clinical cutoff. The clinical cutoff of ImmunoWELL™ Mycoplasma Pneumoniae IgM Test, using a purified CF antigen, is evaluated using presumptively healthy U.S. blood donors.Materials and Methods: Fourteen hundred twenty-six (1426) sera collected from potential U.S. blood donors collected at centers located in thirteen states is tested. Tests are performed using ImmunoWELL Mycoplasma IgM Test following package insert instructions.Results: Figure 1 illustrates specific antibody distribution in a U.S. healthy, adult population.Summary: The 95th percentile (736 to 917 units/mL)is consistency with ImmunoWELL’s 950 units/mL clinical cutoff. The 75th percentile is 295-319 units/mL.Figure 1

IntroductionMycoplasma pneumoniae is the causative agent of atypical pneumonia. Sero-diagnosis detects antibodies against either an immunodominant membrane protein or complement fixing (CF) lipid antigens. Because the membrane protein is water soluble and the CF lipid is not water soluble, only one immune reaction type is detected by most assay methods. Additionally, some older serology kits report analytic results (“epidemiological results”) while newer kits are required to report a clinical cutoff.

In the 1980’s, Dr. Stig Jeansson developed an enzyme immunoassay (EIA) method detecting anti-CF. ImmunoWELL (unpublished method). Mycoplasma Pneumoniae IgM Test uses this original design and more recently ImmunoFLOW Mycoplasma Pneumoniae IgM Test also uses the antigen.

Originally, the ImmunoWELL™ Mycoplasma Pneumoniae IgM Test’s clinical cutoff was established using healthy U.S. blood donors and validated in a prospective study comparing its single IgM interpretation to acute and convalescent (“paired serum”) results. This new study illustrates the incidence of Mycoplasma pneumoniae IgM in a similar U.S. healthy adult population.

Methods & Materials

Figure 1 illustrates anti-CF distribution measured using ImmunoWELL Mycoplasma Pneumoniae IgM Test in a presumptively healthy U.S. adult population.

Conclusions These results are substantially

the same as originally observed (1996) to establish the kit’s clinical cutoff.

Using standards defined using th3 IgM semi-quantitative test, a rapid qualitative test using the same M. pneumoniae CF antigen yields correlative results to an alternative qualitative test.

Contact InformationBryan Kiehl ([email protected])Mobile (+1 760-855-8999)

Frequency of Mycoplasma pneumoniae Complement Fixation IgM in a Healthy, Adult Population

B. Kiehl1 and S. Jeansson2

1GenBio, San Diego, 2Oslo University Hospital, Oslo, Norway

Table 1 shows Mycoplasma IgM test results of eighteen clinical specimens using ImmunoCard and ImmunoFLOW, a flow-through test method using the same Mycoplasma pneumoniae CF antigen.

Note: ImmunoFLOW is not available within the U.S.; however it is available in the European Union (CE Mark) and other international markets.

Results

Number of

Specimens

ImmunoCard

ImmunoFLOW

5 Positive Positive13 Negative Negative

Summary Mycoplasma pneumoniae specific antibody is detected in healthy subjects, presumably because of surface antigen cross-reactivity between Mycoplasma species. Prior to commercial test kits with clinical cutoffs defined by prospective clinical study, acute and convalescent sera (“serum pair”) was required for clinical interpretation. A statistical difference between the specimens is used to aid disease diagnosis. To assure specificity, kits with a clinical cutoff (opposed to the analytic cutoff or older kits) are set at a much higher antibody threshold.

This study measures specific IgM in a presumptively healthy population using the semi-quantitative test ImmunoWELL Mycoplasma Pneumoniae IgM. This test detects specific IgM units/m reporting values above 200 units/mL; however, the clinical cutoff is 950 units/mL.

Although presumptively healthy U.S. blood donor adult population is not the intended test population, it is easily tested and used by the manufacturer as a means to assure product performance clinical cutoff consistency. During the initial 1996 ImmunoWELL prospective validation study a similar U.S. blood donor population was tested and reported as expected results. The current study results are more extensive and report substantially the same results.

Table 2 shows the percentile rankings, corresponding to results. The 95-percentile ranking is 807 units/mL (736 to 917 units/mL) which is consistent with ImmunoWELL’s clinical cutoff. It was also shown that by using ImmunoWELL’s semi-quantitative results to establish a qualitative test method (ImmunoFLOW), good correlation to an alternative qualitative clinical test (see Table 1) is seen.

Percentile

Value

95% LCL

95% UCL

99 1458 1226 169995 807 736 91790 607 559 65085 477 435 52880 387 361 41575 319 295 34970 272 250 29365 234 217 24860 199 188 21755 177 165 19050 156 142 16645 132 123 14340 115 106 12435 98 90 10630 82 77 9025 70 63 7620 56 52 6115 44 40 4910 29 24 365 6 0 141 0 0 0

Table 2: Percentile Rank of U.S. healthy adult population expressed in IgM Units

Table 2: ImmunoCard and ImmunoFLOW Comparison

Figure 1: M. pneumoniae IgM Distribution in U.S. Healthy Adult Population