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167 protocols using liaison xl

1

Comprehensive STI Testing Protocol

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Urethral (in case of having a (neo)penis), pharyngeal (in case of giving fellatio), rectal (in case of receptive anal sex) and vaginal (in case of having a (neo)vagina) specimens were tested for Chlamydia trachomatis and Neisseria gonorrhoeae with the Aptima Combo 2 assay (Hologic, Marlborough, Massachusetts, USA). In asymptomatic individuals, urine, rectal and vaginal specimens were self-collected, while in Amsterdam, medical staff collected rectal and/or vaginal specimens in symptomatic individuals. Medical staff collected pharyngeal specimens in all individuals. Those who had not previously tested HIV-positive were tested for HIV unless they actively opted out. HIV antibodies were tested with the HIV Ab/Ag test (LIAISON XL; DiaSorin, Saluggia, Italy) or Advia HIV Ab/Ag combo assay (Advia Centaur; Siemens Healthcare Diagnostics, Erlangen, Germany), and a treponemal test for syphilis serology was performed with the Treponema Screen (LIAISON XL, DiaSorin) or Advia Syphilis Assay (Advia Centaur, Siemens Healthcare Diagnostics).
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2

STI Screening Among Sex Workers

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Sex workers were tested for Chlamydia trachomatis (Ct) (including LGV in case of anorectal Ct in MSW and TSW), Neisseria gonorrhoeae (Ng), and syphilis. All sex workers who had not previously tested HIV-positive were tested for HIV unless they actively opted out. Urine, pharyngeal, rectal, and vaginal specimens were tested for both Ct and Ng with the Aptima Combo 2 assay (Hologic, Marlborough, MA). In asymptomatic visitors both urine, rectal, and vaginal specimens were selfcollected, while in symptomatic visitors medical staff collected rectal specimens. Medical staff collected pharyngeal specimens in all sex workers. The HIV antibodies were tested with the HIV Ab/Ag test (LIAISON XL; Diasorin, Saluggia, Italy), and a treponemal test for syphilis serology was performed with the Treponema Screen (LIAISON XL; Diasorin, Saluggia, Italy). All bacterial STI diagnoses were based on laboratory outcomes of the STI consultation in which the substance questionnaire was taken.
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3

QuantiFERON-TB Gold Plus IGRA Assay

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Interferon-gamma release assay (IGRA) testing was performed using the QuantiFERON-TB Gold Plus (Qiagen) chemiluminescence assay on the Liaison XL automated platform (DiaSorin) based on the manufacturer’s protocol. The Liaison XL (DiaSorin) was used to quantify the concentration of IFN-γ in each sample tube. A result of positive, negative, or indeterminate was made using an algorithm per the manufacturer’s instructions.
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4

Thyroid Function Biomarkers Assessment

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The serum concentrations of FT3, FT4, TSH, TPOAb, and TGAb were detected using the LIAISON XL fully automated chemiluminescence immunoassay analyzer (LIAISON XL, DiaSorin, Italy) and its supporting reagents and calibrators. Each specimen was tested once within the normal quality control range. The reference intervals for TPOAb and TGAb were in accordance with the LIAISON reagent instructions for TPOAb (1–16 IU/mL) and TGAb (0–100 IU/mL).
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5

Screening MSM for STIs and HIV

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Clients were tested for Chlamydia trachomatis (Ct; including lymphogranuloma venereum [LGV] in case anorectal Ct was found), Neisseria gonorrhoeae (Ng), and syphilis. Urethral Gram stain analysis was performed only in male patients with urogenital signs or symptoms (discharge, painful and/or frequent urination). In those with more than 10 polymorph nucleated leucocytes per high-power field in a urethral Gram-stained smear and no infection with Ct and Ng, a definitive diagnosis of nonspecific urethritis (NSU) was made.19 (link) All MSM who had not previously tested HIV positive were tested for HIV unless they actively opted out.
Urine and pharyngeal and rectal specimens were tested for both Ct and Ng using the Aptima Combo 2 assay (Hologic, Marlborough, MA). In asymptomatic MSM, both urine and rectal specimens were self-collected, whereas in symptomatic MSM, medical staff collected rectal specimens. Medical staff collected pharyngeal specimens in all MSM. HIV antibodies were tested using a rapid HIV test (Alere Determine HIV-1/2 antibody test; Medical Co., Ltd.; Chiba, Japan) and the HIV Ab/Ag test (LIAISON XL; Diasorin, Saluggia, Italy), and syphilis serology was performed using the Treponema Screen (LIAISON XL; Diasorin). All bacterial STI diagnoses were based on laboratory outcomes of the STI consultation in which the chemsex questions were asked.
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6

Evaluation of SARS-CoV-2 Antibody Assays

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The DiaSorin Liaison SARS-CoV-2 S1/S2 IgG chemiluminescence assay detects IgG against spike subunits S1 and S2. Samples were analyzed according to the manufacturer’s guidelines on a DiaSorin Liaison XL automated chemiluminescence analyzer (DiaSorin, Saluggia, Italy). A signal of 15 arbitrary units (AU) per ml or higher is defined by the manufacturer as a positive result. The DiaSorin TrimericS IgG assay applies the soluble trimeric form of the S1/S2 subunits. Samples were analyzed on a DiaSorin Liaison XL automated chemiluminescence analyzer. A signal of 13 AU/ml is defined as a positive result. The Roche electrochemiluminescence immunoassay measures total immunoglobulins against SARS-CoV-2 nucleocapsid (N) protein. Samples were analyzed according to the manufacturer’s guidelines using the Elecsys Anti-SARS-CoV-2 assay on the Roche cobas e602 platform (Roche Diagnostics). A cutoff index (COI) of 1.0 or higher is defined by the manufacturer as a positive result. The Ortho COVID-19 IgG antibody test was performed on Ortho’s VITROS system. The signal-at-cutoff (S/C) value as defined by the manufacturer is 1 unit or greater for a reactive sample. For simplicity, all values of the commercial assays are reported in arbitrary units.
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7

Thyroid Autoantibodies and Embryo Transfer

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Serum thyroid autoantibodies were measured in all patients. Thyroid-stimulating hormone (TSH) was determined in serum on the day of the pretreatment protocol starting (T0). Serum TSH was also quantified 14 days after embryo transfer (T1). At T1, serum beta-hCG was also measured. All laboratory assays were performed at the same laboratory: TSH was measured by electrochemiluminescent assays on an automatic platform (Cobas C 702; Roche Diagnostics, Milan, Italy); antithyroid antibody assays were performed by an automated chemiluminescent method on a Liaison XL (DiaSorin, Saluggia, Italy).
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8

Thyroid Function and Autoantibody Assessment

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Thyroid function tests were measured with an automated direct chemiluminescent method (Advia Centaur XP, Siemens Healthcare Diagnostics, Munich, Germany; normal range: TSH 0.55 to 4.78 µIU/mL, free T4 0.89 to 1.76 ng/dL, and total triiodothyronine [T3] 60 to 181 ng/dL). Thyroid autoantibody assays were also performed by an automated chemiluminescent method (Liaison XL, DiaSorin, Saluggia, Italy; normal range: TRAb 0 to 1.75 IU/L, TPOAb 0 to 60 U/mL, and TgAb 0 to 100 IU/mL).
TRAb, TPOAb, and TgAb were measured at the initial diagnosis and at the time of ATD withdrawal.
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9

Comprehensive Viral Serology Screening

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Serum samples were screened for HIV antibody/antigen, HBV surface antigen (HBsAg) and HCV antibody via ADVIA-Centaur-CP assay (Siemens Healthineers). Any reactive serology results had confirmatory testing via the LIAISON® XL (DiaSorin). Samples reactive on first- and second-line HIV antibody/antigen assays were tested using the Geenius (Bio-Rad Laboratories) to differentiate between HIV-1 and HIV-2. Confirmed positive HBsAg samples were tested for core antibody, e-antigen and e-antibody. Confirmed positive HCV antibody samples were reflex tested for HCV RNA on the Alinity M (Abbott Molecular) to be able to differentiate between those with past and current infection.
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10

SARS-CoV-2 IgG Antibody Detection by Liaison CLIA

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The Liaison SARS-CoV-2 kit, an indirect CLIA, was assayed on a Liaison XL analyzer (Diasorin, Saluggia, Italy). The sample is first incubated with magnetic microbeads coated with recombinant spike S1/S2 antigen. Mouse monoclonal antibodies directed against human IgG are then added. The chemiluminescence signal produced is measured and the concentration of IgG anti S1/S2 is reported in arbitrary units (AU/mL). Results are interpreted as follows: <12 AU/mL = negative, ≥12 to <15 = borderline, ≥15 = positive. Borderline data were considered positive for the statistical analyses.
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