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Neopterin

is a small molecule with a low molecular weight (253.21 g/mol) and belongs to the group known as pteridines. It is synthesized upon a cellular immune reaction. When macrophages and dendritic cells are stimulated by interferon-ɣ, neopterin is released. Neopterin values reflect the entire immunological processes for monocytes/ macrophages and dendritic cells and can be seen as a global immune response marker.

Neopterin Figure1

Figure 1: Release of Neopterin during cellular immune reaction [1].

An increase in neopterin concentration marks the onset of an infection in the body before antibodies are present. As soon as the immune system is triggered by interferon-ɣ, neopterin is released by macrophages.

Neopterin is related to [2]:

  • Early indication of viral infections (e.g. SARS-CoV-2, HIV)
  • Differentiation of acute viral and bacterial infections
  • Indications for autoimmune diseases (e.g. Sjörgren-syndrome, rheumatic diseases)
  • Early indication of complications in allograft rejection episodes
  • Follow-up control of chronic infections, therapy and treatment

Insights and cues from neopterin: Synthesized upon stimulation of macrophages and dendritic cells, neopterin is an early, well-characterized biochemical marker of an ongoing immune reaction to viral infection [2]. 

Neopterin Figure1

Figure 2: Schematic time course of neopterin concentration in blood in relation to the rise and fall of antibody presence in response to viral infection [2].

Measurement in bodily fluids: The determination of neopterin levels in human body fluids offers a useful and innovative tool to monitor diseases associated with the activation of cell-mediated immunity. The ELISA is validated for measuring Neopterin in serum, plasma (EDTA). Neopterin has a higher stability in body fluids which makes the sample handling and measurement easier compared to other cytokines. The low molecular weight, enables Neopterin molecules to pass rapidly through the intravasacular area, where it is released into urine after glomerular filtration. The half-life in the human body is only affected by renal excretion.

Increasing Neopterin levels in various infections precede the clinical manifestation and seroconversion. Normally samples are not tested for all possible infections. Therefore, the measurement of Neopterin in blood donor samples is a useful tool in order to reduce the risk of infections via blood transfusion [2].

Neopterin is helpful since it allows an immediate response for interventions during the early phase of the “diagnostic window”, which indicates the timespan of pathogen invasion and onset of antibodies. Due to the early increase of neopterin therapeutic measures can be taken before the appearance of the antibodies.

Other diagnostic applications Tecan Neopterin Blood Bank ELISA:

  • Aid in screening of blood donors
  • measurements of neopterin levels as an unspecific marker for immune activation or other disturbances of the immune system

Tecan Neopterin Blood Bank ELISA:

Enzyme Immunoassay for the quantitative determination of neopterin.

  • sample type: serum, plasma (EDTA)
  • sample volume: 10 µL
  • Incubation time: 1 x1 h, 1 x 30 min
  • Measuring range: 1.35-111 nmol/L
  • substrate: TMB 450 nm
  • validated and automated for use with Diasorin ETI-Max 3000 ELISA processor

For concrete data please consult the Instruction for Use in the download box on the top right side.

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Our comprehensive immunoassay portfolio includes a number of specialty diagnostic immunoassays for endocrinology, immunology and autoimmunity, as well as for diagnosis of multiple infectious diseases. We are pioneers and market leaders in saliva diagnostics, with over 40 years of experience supplying a broad portfolio of luminescence- and ELISA-based tests, including our highly acclaimed HMGB1 and MuSK-Ab ELISAs.

And as experts in laboratory automation, we can support our customers with the protocols for open ELISA platforms, such as the Freedom EVOlyzer or Thunderbolt®.

All products are only available for sale to laboratory professionals and may not be available in all countries. Availability and regulatory status may vary across regions depending on local country-specific registration. Please always read and follow the instructions for use. 

All of our assays have been designed and manufactured to meet the highest global regulatory requirements and quality standards. Tecan is certified under ISO 9001:2015, ISO 13485:2016 and is audited by a notified body according to Medical Device Single Audit Program (MDSAP).

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