Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Immunotoxicity

Currently viewing:

Administrative data

Endpoint:
immunotoxicity
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
documentation insufficient for assessment

Data source

Referenceopen allclose all

Reference Type:
other: publication [Smialowicz1991a]
Title:
Unnamed
Year:
1991
Reference Type:
other: publication [Smialowicz1991b]
Title:
Immunotoxicity of 2-methoxyethanol following oral administration in Fischer 344 rats
Author:
Smialowicz RJ, Riddle MM, Luebke RW, Copeland CB, Andrews D, Rogers RR, Gray LE, Laskey JW
Year:
1991
Bibliographic source:
Toxicol Appl Pharmacol., 109: 494-506.

Materials and methods

Test material

Constituent 1
Chemical structure
Reference substance name:
Methoxyacetic acid
EC Number:
210-894-6
EC Name:
Methoxyacetic acid
Cas Number:
625-45-6
Molecular formula:
C3H6O3
IUPAC Name:
2-methoxyacetic acid
Constituent 2
Reference substance name:
2-methoxyacetic acid
IUPAC Name:
2-methoxyacetic acid

Results and discussion

Applicant's summary and conclusion

Executive summary:

F344 rats received 10 consecutive daily oral doses of Methoxyacetic acid ranging from 25 to 400 mg/kg bw in several experiments with somewhat diverging dosing regimens. At 100 and 200 mg/kg bw, thymic involution was observed in the absence of body weight reduction; there was also a reduction of lympho-proliferative responses to mitogens (Con A, PHA and PWM). At 200 mg/kg bw, the in vitro generated cytotoxic T-lymphocyte response was reduced, whereas mixed lymphocyte reaction and NKA were unaffected. The PFC response to TNP-LPS was suppressed throughout all dose levels, while increased to SRBC at 50 mg/kgbw. TNP-LPS- and SRBC-immunised rats dosed with Methoxyacetic acid showed suppression of PFC responses at 100 or 200 mg/kg bw and 200 or 400 mg/kg bw, respectively. Phenotypic analysis of splenocytes revealed a small (3%) reduction in the percentage of W3/25-positive cells (i.e. CD4, helper/inducer cells). Spleen cellularity appeared to be unaffected. Interleukin-2 production was decreased in the 150mg/kg bw group (Smialowicz et al, 1991a/b).